rs7641175

This is a intron variant variant.

GWAS Catalog Trait Associations (13)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

platelet glycoprotein 4 level

Pietzner M et al. Mapping the proteo-genomic convergence of human diseases. Science (new York, N.y.) 374(6569):eabj1541 (2021)
Allele A
OR 0.20
p 5.0e-34
N 10,708
Large GWAS
European

platelet volume

Vuckovic D et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell 182(5):1214-1231.e11 (2020)
Allele A
OR 0.03
p 1.0e-30
N 408,112
Large GWAS
European
Allele A
OR 0.04
p 4.0e-18
N 164,454
Large GWAS
European

nidogen-2 measurement

Allele A
OR 0.06
p 2.0e-22
N 47,745
Large GWAS
European

proheparin-binding EGF-like growth factor level

Allele A
OR 0.05
p 2.0e-15
N 47,745
Large GWAS
European

Kunitz-type protease inhibitor 2 measurement

Allele A
OR 0.05
p 7.0e-15
N 47,745
Large GWAS
European

nidogen-1 measurement

Allele A
OR 0.05
p 6.0e-14
N 47,745
Large GWAS
European

vascular endothelial growth factor A level

Allele A
OR 0.04
p 2.0e-13
N 47,745
Large GWAS
European

level of R-spondin-1 in blood serum

Allele A
OR 0.05
p 3.0e-13
N 47,745
Large GWAS
European

level of CCN family member 4 in blood

Allele A
OR 0.04
p 7.0e-13
N 47,745
Large GWAS
European

fibroblast growth factor 2 level

Allele A
OR 0.04
p 2.0e-12
N 47,745
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.

Community Wiki

No community notes yet for this variant. Sign in to start one.

Comments

Sign in to join the discussion.

Loading comments…