rs713875

This variant is located in the HORMAD2 gene.

GWAS Catalog Trait Associations (5)

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

cup-to-disc ratio measurement

Allele C
OR 0.01
p 5.0e-24
N 65,680
Large GWAS
European
Allele C
OR 0.01
p 9.0e-14
N 67,040
Large GWAS
European

body height

Allele G
OR 0.01
p 6.0e-24
N 394,642
Large GWAS
European
Allele G
OR 0.01
p 6.0e-21
N 405,540
Large GWAS
European

disorder of pharynx

Allele G
OR 1.08
p 7.0e-18
N 232,365
Large GWAS
European

aspartate aminotransferase to alanine aminotransferase ratio

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 7.0e-13
N 561,706
Major Consortium StudyLarge GWAS
multi-ancestry

Crohn's disease

Allele C
OR 1.08
p 7.0e-12
N 21,389
Meta-analysisLarge GWAS
European

About HORMAD2

Predicted to be involved in meiotic cell cycle and meiotic sister chromatid cohesion. Located in centrosome; cytosol; and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]

View all HORMAD2 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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