rs9332661

GWAS Catalog Trait Associations (5)

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

solute carrier family 22 member 16 measurement

Pietzner M et al. Mapping the proteo-genomic convergence of human diseases. Science (new York, N.y.) 374(6569):eabj1541 (2021)
Allele A
OR 0.71
p 9.0e-138
N 10,708
Large GWAS
European

protein measurement

Pietzner M et al. Mapping the proteo-genomic convergence of human diseases. Science (new York, N.y.) 374(6569):eabj1541 (2021)
Allele A
OR 0.52
p 4.0e-71
N 10,708
Large GWAS
European
Allele A
OR 0.81
p 2.0e-60
N 3,506
Large GWAS
European

cytochrome c oxidase subunit 6C measurement

Pietzner M et al. Mapping the proteo-genomic convergence of human diseases. Science (new York, N.y.) 374(6569):eabj1541 (2021)
Allele A
OR 0.50
p 6.0e-68
N 10,708
Large GWAS
European

T-cell surface glycoprotein CD3 epsilon chain measurement

Pietzner M et al. Mapping the proteo-genomic convergence of human diseases. Science (new York, N.y.) 374(6569):eabj1541 (2021)
Allele A
OR 0.29
p 6.0e-25
N 10,708
Large GWAS
European

blood protein amount

Allele G
OR 0.38
p 4.0e-12
N 5,356
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…