rs16881446, HS3ST1

N. diseases: 2
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
0.700 SusceptibilityMutation CLINVAR Assessing the function of genetic variants in candidate gene association studies. 15266341 2004
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
0.700 SusceptibilityMutation CLINVAR Assessing the function of genetic variants in candidate gene association studies. 15266341 2004