rs5934505

This is a intergenic variant variant.

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GWAS Catalog Trait Associations (9)

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

testosterone measurement

Fantus RJ et al. “Genetic Susceptibility for Low Testosterone in Men and Its Implications in Biology and Screening: Data from the UK Biobank.” European Urology Open Science 29:36-46 (2021)
Allele T
OR 1.57
p 2.0e-108
N 111,676
Major Consortium StudyLarge GWAS
European
Jin G et al. “Genome-wide association study identifies a new locus JMJD1C at 10q21 that may influence serum androgen levels in men.” Human Molecular Genetics 21(23):5222-8 (2012)
Allele T
OR 0.09
p 2.0e-8
N 3,225
Large GWAS
European

hemoglobin measurement

Vuckovic D et al. “The Polygenic and Monogenic Basis of Blood Traits and Diseases.” Cell 182(5):1214-1231.e11 (2020)
Allele C
OR 0.04
p 9.0e-71
N 408,112
Large GWAS
European

hematocrit

Vuckovic D et al. “The Polygenic and Monogenic Basis of Blood Traits and Diseases.” Cell 182(5):1214-1231.e11 (2020)
Allele C
OR 0.04
p 5.0e-68
N 408,112
Large GWAS
European

serum creatinine amount

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 3.0e-18
N 494,370
Large GWAS
multi-ancestry

alopecia

Hagenaars SP et al. “Genetic prediction of male pattern baldness.” Plos Genetics 13(2):e1006594 (2017)
Allele C
OR —
β 0.082
p 2.0e-14
N 52,874
Large GWAS
European

lipoprotein measurement

Zoodsma M et al. “A genetic map of human metabolism across the allele frequency spectrum.” Nature Genetics 57(10):2445-2455 (2025)
Allele C
OR 0.02
p 3.0e-14
N 203,300
Large GWAS
European

high density lipoprotein cholesterol measurement

Zoodsma M et al. “A genetic map of human metabolism across the allele frequency spectrum.” Nature Genetics 57(10):2445-2455 (2025)
Allele C
OR 0.02
p 2.0e-13
N 203,300
Large GWAS
European

androgenetic alopecia

Pirastu N et al. “GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk.” Nature Communications 8(1):1584 (2017)
Allele T
OR 0.16
p 4.0e-13
N 43,590
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.

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