{"count":12,"next":null,"previous":null,"results":[{"gene_data":{"alias":["BAF47","Ini1","Snr1","hSNFS","Sfh1p","RDT","PPP1R144"],"biotype":"protein_coding","hgnc_id":"HGNC:11103","gene_name":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1","omim_gene":["601607"],"alias_name":["sucrose nonfermenting, yeast, homolog-like 1","integrase interactor 1","malignant rhabdoid tumor suppressor","protein phosphatase 1, regulatory subunit 144"],"gene_symbol":"SMARCB1","hgnc_symbol":"SMARCB1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"22:24129150-24176703","ensembl_id":"ENSG00000099956"}},"GRch38":{"90":{"location":"22:23786963-23834516","ensembl_id":"ENSG00000099956"}}},"hgnc_date_symbol_changed":"1995-08-21"},"entity_type":"gene","entity_name":"SMARCB1","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":["PubMed: 18285426"],"evidence":["Expert Review Green","UKGTN","Illumina TruGenome Clinical Sequencing Services"],"phenotypes":["Schwannomatosis","(originally on Familial schwannomatosis gene panel)"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","tags":[],"panel":{"id":167,"hash_id":"55af764522c1fc78a829f89a","name":"Familial Tumours Syndromes of the central & peripheral Nervous system","disease_group":"Tumour syndromes","disease_sub_group":"Muscle and nerve","status":"public","version":"1.9","version_created":"2019-06-20T15:11:10.374253Z","relevant_disorders":["Familial tumour syndromes of the central & peripheral nervous system","Familial tumour syndromes of the central and peripheral nervous system"],"stats":{"number_of_genes":21,"number_of_strs":0,"number_of_regions":1},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["BAF47","Ini1","Snr1","hSNFS","Sfh1p","RDT","PPP1R144"],"biotype":"protein_coding","hgnc_id":"HGNC:11103","gene_name":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1","omim_gene":["601607"],"alias_name":["sucrose nonfermenting, yeast, homolog-like 1","integrase interactor 1","malignant rhabdoid tumor suppressor","protein phosphatase 1, regulatory subunit 144"],"gene_symbol":"SMARCB1","hgnc_symbol":"SMARCB1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"22:24129150-24176703","ensembl_id":"ENSG00000099956"}},"GRch38":{"90":{"location":"22:23786963-23834516","ensembl_id":"ENSG00000099956"}}},"hgnc_date_symbol_changed":"1995-08-21"},"entity_type":"gene","entity_name":"SMARCB1","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":null,"publications":[],"evidence":["Expert list","Expert Review Green"],"phenotypes":["Atypical rhabdoid tumor predisposition"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":391,"hash_id":null,"name":"Adult solid tumours for rare disease","disease_group":"Tumour syndromes","disease_sub_group":"Tumour syndromes","status":"public","version":"1.22","version_created":"2019-06-20T15:10:02.142139Z","relevant_disorders":["Young adult onset cancer","Exceptionally young adult onset cancer","Multiple Tumours","Rare tumour predisposition syndromes"],"stats":{"number_of_genes":58,"number_of_strs":0,"number_of_regions":1},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["BAF47","Ini1","Snr1","hSNFS","Sfh1p","RDT","PPP1R144"],"biotype":"protein_coding","hgnc_id":"HGNC:11103","gene_name":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1","omim_gene":["601607"],"alias_name":["sucrose nonfermenting, yeast, homolog-like 1","integrase interactor 1","malignant rhabdoid tumor suppressor","protein phosphatase 1, regulatory subunit 144"],"gene_symbol":"SMARCB1","hgnc_symbol":"SMARCB1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"22:24129150-24176703","ensembl_id":"ENSG00000099956"}},"GRch38":{"90":{"location":"22:23786963-23834516","ensembl_id":"ENSG00000099956"}}},"hgnc_date_symbol_changed":"1995-08-21"},"entity_type":"gene","entity_name":"SMARCB1","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":["12016529"],"evidence":["NHS GMS","Expert List","Expert Review Green","Expert list"],"phenotypes":["Atypical rhabdoid tumor predisposition","609322"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":243,"hash_id":"55af539322c1fc78a9ef5052","name":"Tumour predisposition - childhood onset","disease_group":"Tumour syndromes","disease_sub_group":"Childhood Tumours","status":"public","version":"1.36","version_created":"2019-08-12T08:35:21.843722Z","relevant_disorders":["Paediatric congenital malformation-dysmorphism-tumour syndrome","Paediatric congenital malformation-dysmorphism-tumour syndromes","Paediatric congenital malformation-dysmorphism-tumour sydromes","Paediatric congenital malformation-dysmorphism-tumour syndrome","R359"],"stats":{"number_of_genes":113,"number_of_strs":0,"number_of_regions":1},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"},{"name":"GMS Rare Disease Virtual","slug":"gms-rare-disease-virtual","description":"This is a panel for the Genomic Medicine Service for an exome/genome/panel based test that requires a virtual gene panel for rare disease in the Test Directory."},{"name":"GMS Cancer Germline Virtual","slug":"gms-cancer-germline-virtual","description":"This is a panel used for WGS germline analysis for the GMS."}]}},{"gene_data":{"alias":["BAF47","Ini1","Snr1","hSNFS","Sfh1p","RDT","PPP1R144"],"biotype":"protein_coding","hgnc_id":"HGNC:11103","gene_name":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1","omim_gene":["601607"],"alias_name":["sucrose nonfermenting, yeast, homolog-like 1","integrase interactor 1","malignant rhabdoid tumor suppressor","protein phosphatase 1, regulatory subunit 144"],"gene_symbol":"SMARCB1","hgnc_symbol":"SMARCB1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"22:24129150-24176703","ensembl_id":"ENSG00000099956"}},"GRch38":{"90":{"location":"22:23786963-23834516","ensembl_id":"ENSG00000099956"}}},"hgnc_date_symbol_changed":"1995-08-21"},"entity_type":"gene","entity_name":"SMARCB1","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Green","NHS GMS","Expert Review"],"phenotypes":[],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":600,"hash_id":null,"name":"Rhabdoid tumour predisposition","disease_group":"","disease_sub_group":"","status":"public","version":"1.0","version_created":"2019-08-16T10:05:20.097569Z","relevant_disorders":["R358"],"stats":{"number_of_genes":2,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"GMS Rare Disease","slug":"gms-rare-disease","description":"This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"},{"name":"GMS signed-off","slug":"gms-signed-off","description":"This panel has undergone review by a NHSE GMS disease specialist group and processes to be signed-off for use within the GMS."}]}},{"gene_data":{"alias":["BAF47","Ini1","Snr1","hSNFS","Sfh1p","RDT","PPP1R144"],"biotype":"protein_coding","hgnc_id":"HGNC:11103","gene_name":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1","omim_gene":["601607"],"alias_name":["sucrose nonfermenting, yeast, homolog-like 1","integrase interactor 1","malignant rhabdoid tumor suppressor","protein phosphatase 1, regulatory subunit 144"],"gene_symbol":"SMARCB1","hgnc_symbol":"SMARCB1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"22:24129150-24176703","ensembl_id":"ENSG00000099956"}},"GRch38":{"90":{"location":"22:23786963-23834516","ensembl_id":"ENSG00000099956"}}},"hgnc_date_symbol_changed":"1995-08-21"},"entity_type":"gene","entity_name":"SMARCB1","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["18285426"],"evidence":["Expert Review Green","Familial Tumours Syndromes of the central & peripheral Nervous system (Version 1.8)","Adult solid tumours for rare disease (Version 1.21)"],"phenotypes":["(originally on Familial schwannomatosis gene panel)","Schwannomatosis","Atypical rhabdoid tumor predisposition"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":470,"hash_id":null,"name":"Tumour predisposition - adult onset","disease_group":"","disease_sub_group":"","status":"public","version":"1.1","version_created":"2019-06-20T15:14:23.703488Z","relevant_disorders":[],"stats":{"number_of_genes":63,"number_of_strs":0,"number_of_regions":2},"types":[{"name":"GMS Rare Disease Virtual","slug":"gms-rare-disease-virtual","description":"This is a panel for the Genomic Medicine Service for an exome/genome/panel based test that requires a virtual gene panel for rare disease in the Test Directory."}]}},{"gene_data":{"alias":["BAF47","Ini1","Snr1","hSNFS","Sfh1p","RDT","PPP1R144"],"biotype":"protein_coding","hgnc_id":"HGNC:11103","gene_name":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1","omim_gene":["601607"],"alias_name":["sucrose nonfermenting, yeast, homolog-like 1","integrase interactor 1","malignant rhabdoid tumor suppressor","protein phosphatase 1, regulatory subunit 144"],"gene_symbol":"SMARCB1","hgnc_symbol":"SMARCB1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"22:24129150-24176703","ensembl_id":"ENSG00000099956"}},"GRch38":{"90":{"location":"22:23786963-23834516","ensembl_id":"ENSG00000099956"}}},"hgnc_date_symbol_changed":"1995-08-21"},"entity_type":"gene","entity_name":"SMARCB1","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":["12016529"],"evidence":["Expert Review Green","Expert list"],"phenotypes":["Atypical rhabdoid tumor predisposition"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":259,"hash_id":"595cd7cc8f62036352471ea1","name":"Childhood solid tumours cancer susceptibility","disease_group":"Cancer Programme","disease_sub_group":"Pertinent cancer susceptibility gene panel","status":"public","version":"1.5","version_created":"2019-08-13T09:49:07.790050Z","relevant_disorders":["Childhood;Childhood solid tumours pertinent cancer susceptibility"],"stats":{"number_of_genes":83,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Cancer Germline 100K","slug":"cancer-germline-100k","description":"Cancer Germline 100K"}]}},{"gene_data":{"alias":["BAF47","Ini1","Snr1","hSNFS","Sfh1p","RDT","PPP1R144"],"biotype":"protein_coding","hgnc_id":"HGNC:11103","gene_name":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1","omim_gene":["601607"],"alias_name":["sucrose nonfermenting, yeast, homolog-like 1","integrase interactor 1","malignant rhabdoid tumor suppressor","protein phosphatase 1, regulatory subunit 144"],"gene_symbol":"SMARCB1","hgnc_symbol":"SMARCB1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"22:24129150-24176703","ensembl_id":"ENSG00000099956"}},"GRch38":{"90":{"location":"22:23786963-23834516","ensembl_id":"ENSG00000099956"}}},"hgnc_date_symbol_changed":"1995-08-21"},"entity_type":"gene","entity_name":"SMARCB1","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["NHS GMS","Expert Review Green","Expert list"],"phenotypes":["Atypical rhabdoid tumor predisposition"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":245,"hash_id":"595ce30f8f62036352471f39","name":"Adult solid tumours cancer susceptibility","disease_group":"Cancer Programme","disease_sub_group":"Pertinent cancer susceptibility gene panel","status":"public","version":"1.7","version_created":"2019-08-13T09:55:08.772098Z","relevant_disorders":["Carcinoma of unknown primary","Other","Adult solid tumours pertinent cancer susceptibility"],"stats":{"number_of_genes":103,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Cancer Germline 100K","slug":"cancer-germline-100k","description":"Cancer Germline 100K"},{"name":"GMS Cancer Germline Virtual","slug":"gms-cancer-germline-virtual","description":"This is a panel used for WGS germline analysis for the GMS."}]}},{"gene_data":{"alias":["BAF47","Ini1","Snr1","hSNFS","Sfh1p","RDT","PPP1R144"],"biotype":"protein_coding","hgnc_id":"HGNC:11103","gene_name":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1","omim_gene":["601607"],"alias_name":["sucrose nonfermenting, yeast, homolog-like 1","integrase interactor 1","malignant rhabdoid tumor suppressor","protein phosphatase 1, regulatory subunit 144"],"gene_symbol":"SMARCB1","hgnc_symbol":"SMARCB1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"22:24129150-24176703","ensembl_id":"ENSG00000099956"}},"GRch38":{"90":{"location":"22:23786963-23834516","ensembl_id":"ENSG00000099956"}}},"hgnc_date_symbol_changed":"1995-08-21"},"entity_type":"gene","entity_name":"SMARCB1","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":[""],"phenotypes":["Coffin Siris syndrome"],"mode_of_inheritance":"","tags":[],"panel":{"id":309,"hash_id":"5693952f22c1fc251660fb1e","name":"Skeletal dysplasia","disease_group":"Skeletal disorders","disease_sub_group":"Skeletal dysplasias","status":"public","version":"1.203","version_created":"2019-10-03T09:38:50.417968Z","relevant_disorders":["Unexplained skeletal dysplasia","Skeletal dysplasia"],"stats":{"number_of_genes":546,"number_of_strs":1,"number_of_regions":6},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"},{"name":"GMS Rare Disease Virtual","slug":"gms-rare-disease-virtual","description":"This is a panel for the Genomic Medicine Service for an exome/genome/panel based test that requires a virtual gene panel for rare disease in the Test Directory."},{"name":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}},{"gene_data":{"alias":["BAF47","Ini1","Snr1","hSNFS","Sfh1p","RDT","PPP1R144"],"biotype":"protein_coding","hgnc_id":"HGNC:11103","gene_name":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1","omim_gene":["601607"],"alias_name":["sucrose nonfermenting, yeast, homolog-like 1","integrase interactor 1","malignant rhabdoid tumor suppressor","protein phosphatase 1, regulatory subunit 144"],"gene_symbol":"SMARCB1","hgnc_symbol":"SMARCB1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"22:24129150-24176703","ensembl_id":"ENSG00000099956"}},"GRch38":{"90":{"location":"22:23786963-23834516","ensembl_id":"ENSG00000099956"}}},"hgnc_date_symbol_changed":"1995-08-21"},"entity_type":"gene","entity_name":"SMARCB1","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["PAGE DD-Gene2Phenotype","Expert Review Green"],"phenotypes":["RHABDOID PREDISPOSITION SYNDROME 1","?COFFIN-SIRIS SYNDROME"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":478,"hash_id":null,"name":"Fetal anomalies","disease_group":"","disease_sub_group":"","status":"public","version":"0.344","version_created":"2019-09-17T09:38:10.568007Z","relevant_disorders":["R21"],"stats":{"number_of_genes":1721,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"GMS Rare Disease Virtual","slug":"gms-rare-disease-virtual","description":"This is a panel for the Genomic Medicine Service for an exome/genome/panel based test that requires a virtual gene panel for rare disease in the Test Directory."}]}},{"gene_data":{"alias":["BAF47","Ini1","Snr1","hSNFS","Sfh1p","RDT","PPP1R144"],"biotype":"protein_coding","hgnc_id":"HGNC:11103","gene_name":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1","omim_gene":["601607"],"alias_name":["sucrose nonfermenting, yeast, homolog-like 1","integrase interactor 1","malignant rhabdoid tumor suppressor","protein phosphatase 1, regulatory subunit 144"],"gene_symbol":"SMARCB1","hgnc_symbol":"SMARCB1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"22:24129150-24176703","ensembl_id":"ENSG00000099956"}},"GRch38":{"90":{"location":"22:23786963-23834516","ensembl_id":"ENSG00000099956"}}},"hgnc_date_symbol_changed":"1995-08-21"},"entity_type":"gene","entity_name":"SMARCB1","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["25249037","23929686","22726846","23906836","23815551","29907796","22426308"],"evidence":["DD-Gene2Phenotype","Expert Review Green"],"phenotypes":["EHMT1-like SYNDROME","RHABDOID PREDISPOSITION SYNDROME 1 609322"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":484,"hash_id":null,"name":"DDG2P","disease_group":"","disease_sub_group":"","status":"public","version":"1.137","version_created":"2019-10-08T15:56:59.220133Z","relevant_disorders":[],"stats":{"number_of_genes":1893,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"GMS Rare Disease","slug":"gms-rare-disease","description":"This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"},{"name":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}},{"gene_data":{"alias":["BAF47","Ini1","Snr1","hSNFS","Sfh1p","RDT","PPP1R144"],"biotype":"protein_coding","hgnc_id":"HGNC:11103","gene_name":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1","omim_gene":["601607"],"alias_name":["sucrose nonfermenting, yeast, homolog-like 1","integrase interactor 1","malignant rhabdoid tumor suppressor","protein phosphatase 1, regulatory subunit 144"],"gene_symbol":"SMARCB1","hgnc_symbol":"SMARCB1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"22:24129150-24176703","ensembl_id":"ENSG00000099956"}},"GRch38":{"90":{"location":"22:23786963-23834516","ensembl_id":"ENSG00000099956"}}},"hgnc_date_symbol_changed":"1995-08-21"},"entity_type":"gene","entity_name":"SMARCB1","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Victorian Clinical Genetics Services","Expert Review Green","Radboud University Medical Center, Nijmegen"],"phenotypes":["Rhabdoid tumors, somatic, 609322Rhabdoid predisposition syndrome 1, 609322Mental retardation, autosomal dominant 15, 614608","RHABDOID PREDISPOSITION SYNDROME 1"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","tags":[],"panel":{"id":285,"hash_id":"558aa423bb5a16630e15b63c","name":"Intellectual disability","disease_group":"Neurology and neurodevelopmental disorders","disease_sub_group":"Neurodevelopmental disorders","status":"public","version":"2.1065","version_created":"2019-10-07T13:42:16.019766Z","relevant_disorders":["Coarse facial features including Coffin-Siris-like disorders","ID","Moderate","severe or profound intellectual disability","Schizophrenia plus additional features","Intellectual disability - microarray","fragile X and sequencing"],"stats":{"number_of_genes":2253,"number_of_strs":11,"number_of_regions":57},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"},{"name":"GMS Rare Disease Virtual","slug":"gms-rare-disease-virtual","description":"This is a panel for the Genomic Medicine Service for an exome/genome/panel based test that requires a virtual gene panel for rare disease in the Test Directory."},{"name":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}},{"gene_data":{"alias":["BAF47","Ini1","Snr1","hSNFS","Sfh1p","RDT","PPP1R144"],"biotype":"protein_coding","hgnc_id":"HGNC:11103","gene_name":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1","omim_gene":["601607"],"alias_name":["sucrose nonfermenting, yeast, homolog-like 1","integrase interactor 1","malignant rhabdoid tumor suppressor","protein phosphatase 1, regulatory subunit 144"],"gene_symbol":"SMARCB1","hgnc_symbol":"SMARCB1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"22:24129150-24176703","ensembl_id":"ENSG00000099956"}},"GRch38":{"90":{"location":"22:23786963-23834516","ensembl_id":"ENSG00000099956"}}},"hgnc_date_symbol_changed":"1995-08-21"},"entity_type":"gene","entity_name":"SMARCB1","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["NHS GMS","Expert Review Amber","Expert list"],"phenotypes":["Rhabdoid tu, schwannomatosis"],"mode_of_inheritance":"","tags":[],"panel":{"id":734,"hash_id":null,"name":"Sarcoma susceptibility","disease_group":"","disease_sub_group":"","status":"public","version":"0.10","version_created":"2019-08-06T10:07:36.980082Z","relevant_disorders":[],"stats":{"number_of_genes":42,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"GMS Cancer Germline Virtual","slug":"gms-cancer-germline-virtual","description":"This is a panel used for WGS germline analysis for the GMS."}]}}]}