rs217181

GWAS Catalog Trait Associations (21)

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

apolipoprotein L1 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 0.34
p 2.0e-92
N 10,708
Large GWAS
European

haptoglobin measurement

Allele T
OR 0.96
p 1.0e-75
N 997
Small GWAS
multi-ancestry

ferritin measurement

Sun BB et al. Genomic atlas of the human plasma proteome. Nature 558(7708):73-79 (2018)
Allele T
OR 0.52
p 7.0e-69
N 3,301
Large GWAS
European
Allele T
OR 0.45
p 4.0e-16
N 997
Small GWAS
multi-ancestry

level of phosphatidylcholine

Zoodsma M et al. A genetic map of human metabolism across the allele frequency spectrum. Nature Genetics 57(10):2445-2455 (2025)
Allele T
OR 0.02
p 8.0e-25
N 450,015
Large GWAS
multi-ancestry

hemoglobin measurement

Allele T
OR
p 6.0e-19
N 746,431
Large GWAS
multi-ancestry
Allele T
OR 0.01
p 2.0e-12
N 394,642
Large GWAS
European

health trait

Allele C
OR 0.01
p 4.0e-17
N 405,979
Large GWAS
European

melanocyte protein PMEL measurement

Allele T
OR 0.85
p 3.0e-14
N 200
Small GWAS
European

low density lipoprotein cholesterol measurement

Allele C
OR 0.05
p 6.0e-14
N 60,405
Large GWAS
Hispanic or Latin American
Allele C
OR 0.05
p 1.0e-8
N 48,057
Large GWAS
Hispanic or Latin American

hematocrit

Verma A et al. Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele C
OR 0.02
p 9.0e-14
N 407,836
Major Consortium StudyLarge GWAS
European
Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele C
OR 0.01
p 6.0e-13
N 503,490
Large GWAS
multi-ancestry

total cholesterol measurement

Allele C
OR 0.05
p 2.0e-12
N 62,209
Large GWAS
Hispanic or Latin American

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…