rs7166081

GWAS Catalog Trait Associations (9)

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

body fat percentage

Allele A
OR
β 0.016
p 2.0e-20
N 442,278
Large GWAS
European

waist-hip ratio

Allele A
OR 0.02
p 2.0e-16
N 316,772
Meta-analysisLarge GWAS
European

fat pad mass

Harris BHL et al. New role of fat-free mass in cancer risk linked with genetic predisposition. Scientific Reports 14(1):7270 (2024)
Allele A
OR 0.02
p 7.0e-11
N 337,196
Large GWAS
European

eosinophil count

Vuckovic D et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell 182(5):1214-1231.e11 (2020)
Allele A
OR 0.02
p 7.0e-10
N 408,112
Large GWAS
European

BMI-adjusted waist circumference

Allele A
OR 0.02
p 2.0e-9
N 143,480
Large GWAS
multi-ancestry

forced expiratory volume, 25-hydroxyvitamin D3 measurement

Allele G
OR
p 8.0e-9
N 115,312
Meta-analysisLarge GWAS
multi-ancestry

body height

Allele G
OR 0.01
p 1.0e-8
N 472,730
Large GWAS
East Asian

smoking behavior, BMI-adjusted waist circumference

Allele A
OR
p 8.0e-10
N 195,506
Meta-analysisLarge GWAS
multi-ancestry

Research that mentions this SNP (1)

Genome-wide association analysis with selective genotyping identifies candidate loci for adult height at 8q21.13 and 15q22.33-q23 in Mongolians
AssociationN=1,555Tetsuaki Kimura et al.(2008)· Human Genetics

Genome-wide association study in 1,555 Khalkh-Mongolian individuals identified two candidate loci for adult height using selective genotyping and microsatellite/SNP analysis. SNP rs2220456 at 8q21.13 showed the strongest association (P = 0.000016), while SNP rs8038652 in IQCH intron 1 at 15q22.33 was highly significant (P = 0.0003 overall, P = 0.000046 for AA genotype under recessive model, OR = 0.59). The study also identified additional significant SNPs in SMAD3 and FLJ11506 genes in the same region.

Traits studied:Adult height

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…