Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3846662
rs3846662
Entrez Id: 3156
Gene Symbol: HMGCR
HMGCR
CUI: C1445957
Disease:
Serum total cholesterol measurement
0.800 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
dbSNP: rs3846662
rs3846662
Entrez Id: 3156
Gene Symbol: HMGCR
HMGCR
CUI: C1445957
Disease:
Serum total cholesterol measurement
0.800 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs3846662
rs3846662
Entrez Id: 3156
Gene Symbol: HMGCR
HMGCR
CUI: C1445957
Disease:
Serum total cholesterol measurement
G 0.800 GeneticVariation GWASCAT Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. 19060911 2009
dbSNP: rs3846662
rs3846662
Entrez Id: 3156
Gene Symbol: HMGCR
HMGCR
CUI: C1445957
Disease:
Serum total cholesterol measurement
G 0.800 GeneticVariation GWASDB Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. 19060911 2009