Gene: MSH6 ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1553413710
rs1553413710
MSH6 ; FBXO11
T 0.700 CausalMutation CLINVAR A multifactorial likelihood model for MMR gene variant classification incorporating probabilities based on sequence bioinformatics and tumor characteristics: a report from the Colon Cancer Family Registry. 22949379

2013
dbSNP: rs1021631442
rs1021631442
MSH6 ; FBXO11
A 0.700 GeneticVariation CLINVAR Frequency of mutations in mismatch repair genes in a population-based study of women with ovarian cancer. 23047549

2012
dbSNP: rs267608058
rs267608058
MSH6 ; FBXO11
A 0.700 CausalMutation CLINVAR

dbSNP: rs267608078
rs267608078
MSH6 ; FBXO11
AC 0.700 CausalMutation CLINVAR

dbSNP: rs63750767
rs63750767
MSH6 ; FBXO11
TTCAAAAGGGACATAGAAAA 0.700 CausalMutation CLINVAR

dbSNP: rs864622607
rs864622607
MSH6 ; FBXO11
G 0.700 GeneticVariation CLINVAR

dbSNP: rs869312770
rs869312770
MSH6 ; FBXO11
C 0.700 CausalMutation CLINVAR