Source: INFERRED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587779157
rs587779157
MSH2
G 0.700 GeneticVariation CLINVAR Microsatellite Instability Is Associated With the Presence of Lynch Syndrome Pan-Cancer. 30376427

2019
dbSNP: rs587779157
rs587779157
MSH2
G 0.700 GeneticVariation CLINVAR Multigene Panel Testing Provides a New Perspective on Lynch Syndrome. 28514183

2017
dbSNP: rs587779157
rs587779157
MSH2
G 0.700 GeneticVariation CLINVAR Genetic features of Lynch syndrome in the Israeli population. 25430799

2015
dbSNP: rs587779157
rs587779157
MSH2
G 0.700 GeneticVariation CLINVAR Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database. 24362816

2014
dbSNP: rs587779157
rs587779157
MSH2
G 0.700 GeneticVariation CLINVAR Mutation spectrum in HNPCC in the Israeli population. 18389388

2008
dbSNP: rs587779157
rs587779157
MSH2
G 0.700 GeneticVariation CLINVAR DHPLC mutation analysis of the hereditary nonpolyposis colon cancer (HNPCC) genes hMLH1 and hMSH2. 11179758

2001
dbSNP: rs587779157
rs587779157
MSH2
G 0.700 GeneticVariation CLINVAR Novel germline mutation (300-305delAGTTGA) in the human MSH2 gene in hereditary non-polyposis colorectal cancer (HNPCC). 10874318

2000
dbSNP: rs587779157
rs587779157
MSH2
G 0.700 CausalMutation CLINVAR