MSH6, mutS homolog 6, 2956

N. diseases: 296; N. variants: 642
Disease: Hereditary Nonpolyposis Colorectal Cancer ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1553333584
rs1553333584
Entrez Id: 2956;80204
Gene Symbol: MSH6;FBXO11
MSH6;FBXO11
CUI: C1333990
Disease:
Hereditary Nonpolyposis Colorectal Cancer 		GCTAATCTCCCAGAGGAAGTTAT 0.700 CausalMutation CLINVAR