rs12147642
This is a intron variant variant.
▶GWAS Catalog Trait Associations (3)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (3)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
axin-2 measurement
Allele T
OR —
β 1.000
p —
N 3,301
Large GWAS
European
multiple coagulation factor deficiency protein 2 measurement
Allele T
OR —
β 1.160
p —
N 3,301
Large GWAS
European
segment polarity protein dishevelled homolog DVL-2 measurement
Pietzner M et al. “Mapping the proteo-genomic convergence of human diseases.” Science (new York, N.y.) 374(6569):eabj1541 (2021)
Allele T
OR 0.21
p 1.0e-41
N 10,708
Large GWAS
European
This variant is in our database but has no known associations or PRS memberships yet.
Gene information from NCBI Gene. Variant classifications from ClinVar.
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