Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs646776
rs646776
CELSR2
0.800 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584

2019
dbSNP: rs646776
rs646776
CELSR2
G 0.800 GeneticVariation GWASCAT Genome-wide association study of blood lipids in Indians confirms universality of established variants. 30911093

2019
dbSNP: rs646776
rs646776
CELSR2
C 0.800 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422

2018
dbSNP: rs646776
rs646776
CELSR2
0.800 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010

2018
dbSNP: rs646776
rs646776
CELSR2
T 0.800 GeneticVariation GWASCAT The impact of low-frequency and rare variants on lipid levels. 25961943

2015
dbSNP: rs646776
rs646776
CELSR2
0.800 GeneticVariation GWASDB Gene-centric meta-analysis of lipid traits in African, East Asian and Hispanic populations. 23236364

2012
dbSNP: rs646776
rs646776
CELSR2
0.800 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622

2012
dbSNP: rs646776
rs646776
CELSR2
G 0.800 GeneticVariation GWASDB Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. 19060911

2009
dbSNP: rs646776
rs646776
CELSR2
G 0.800 GeneticVariation GWASCAT Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. 19060911

2009