Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs662
rs662
CUI: C1827841
Disease: Enzyme activity finding
Enzyme activity finding
C 0.700 GeneticVariation CLINVAR

dbSNP: rs662
rs662
CORONARY ARTERY DISEASE, SUSCEPTIBILITY TO
C 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs662
rs662
CORONARY ARTERY SPASM 2, SUSCEPTIBILITY TO
C 0.700 SusceptibilityMutation CLINVAR