Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3802230
rs3802230
CYP11B2 ; GML
0.010 GeneticVariation BEFREE Single-locus analysis showed that the C allele of rs3802230 was significantly more prevalent in the EH subj</span>ects as compared to control subjects, adjusted for covariates. 21269059

2011