Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587781628
rs587781628
MUTYH
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		C 0.700 CausalMutation CLINVAR The potential for increased clinical sensitivity in genetic testing for polyposis colorectal cancer through the analysis of MYH mutations in North American patients. 15635083

2005
dbSNP: rs587781628
rs587781628
MUTYH
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		C 0.700 CausalMutation CLINVAR Germline susceptibility to colorectal cancer due to base-excision repair gene defects. 15931596

2005
dbSNP: rs587781628
rs587781628
MUTYH
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		C 0.700 CausalMutation CLINVAR MYH mutations in patients with attenuated and classic polyposis and with young-onset colorectal cancer without polyps. 15236166

2004