Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555877286
rs1555877286
SMARCB1
T 0.700 CausalMutation CLINVAR Whole Exome- and mRNA-Sequencing of an AT/RT Case Reveals Few Somatic Mutations and Several Deregulated Signalling Pathways in the Context of SMARCB1 Deficiency. 26998479

2015
dbSNP: rs1555877286
rs1555877286
SMARCB1
T 0.700 CausalMutation CLINVAR SMARCB1 mutations in schwannomatosis and genotype correlations with rhabdoid tumors. 24933152

2014
dbSNP: rs1555877286
rs1555877286
SMARCB1
T 0.700 CausalMutation CLINVAR Spectrum of SMARCB1/INI1 mutations in familial and sporadic rhabdoid tumors. 21108436

2011
dbSNP: rs1555877286
rs1555877286
SMARCB1
T 0.700 CausalMutation CLINVAR Frequent hSNF5/INI1 germline mutations in patients with rhabdoid tumor. 21208904

2011
dbSNP: rs1555877286
rs1555877286
SMARCB1
T 0.700 CausalMutation CLINVAR Clinicopathologic comparison of familial versus sporadic atypical teratoid/rhabdoid tumors (AT/RT) of the central nervous system. 20848638

2011
dbSNP: rs1555877286
rs1555877286
SMARCB1
T 0.700 CausalMutation CLINVAR Constitutional mutations of the hSNF5/INI1 gene predispose to a variety of cancers. 10521299

1999