rs2167364

▶

GWAS Catalog Trait Associations (3)

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

erythrocyte volume

Loya H et al. “A scalable variational inference approach for increased mixed-model association power.” Nature Genetics 57(2):461-468 (2025)

Allele C

OR 0.02

p 2.0e-17

N 394,642

Large GWAS

European

body height

Yengo L et al. “A saturated map of common genetic variants associated with human height.” Nature 610(7933):704-712 (2022)

Allele C

OR 0.02

p 1.0e-11

N 455,180

Large GWAS

Hispanic or Latin American

acute lymphoblastic leukemia

Ellinghaus E et al. “Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia.” Leukemia 26(5):902-9 (2012)

Allele G

OR 1.32

p 2.0e-8

N 900

Small GWAS

European

▶

Research that mentions this SNP (1)

▶

Replication analysis confirms the association of several variants with acute myeloid leukemia in Chinese population

AssociationN=1,579Songyu Cao et al.(2016)· Journal of Cancer Research and Clinical Oncology

Replication study in a Chinese population confirming associations between 16 SNPs and acute myeloid leukemia (AML) risk identified in European GWAS studies. Seven SNPs showed significant associations with AML susceptibility, including rs2191566 (OR=1.46), rs9290663 (OR=1.26), rs11155133 (OR=1.32), rs10873876 (OR=0.62, protective), rs2239633, rs10821936, and rs2242041, in a case-control study of 545 AML cases and 1034 controls.

Traits studied:AMLAcute myeloid leukemia

PubMed DOI Metascience Observatory

This variant is in our database but has no known associations or PRS memberships yet.