rs3733897
This variant is located in the TXNDC15 gene.
▶GWAS Catalog Trait Associations (2)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (2)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
blood protein amount
Gudjonsson A et al. “A genome-wide association study of serum proteins reveals shared loci with common diseases.” Nature Communications 13(1):480 (2022)
Allele G
OR 0.29
p 2.0e-26
N 5,352
Large GWAS
European
testosterone measurement
Ruth KS et al. “Using human genetics to understand the disease impacts of testosterone in men and women.” Nature Medicine 26(2):252-258 (2020)
Allele A
OR 0.03
p 4.0e-9
N 178,782
Large GWAS
European
▶ClinVar annotation
Benign★☆☆☆
2 submitters1 publicationnot provided; Adrenocortical carcinoma, hereditary; Colorectal cancer; Cholangiocarcinoma; Uveal melanoma; Malignant lymphoma, large B-cell, diffuse; Uterine carcinosarcoma
View on ClinVar →About TXNDC15
This gene encodes a member of the thioredoxin superfamily. Members of this family are characterized by a conserved active motif called the thioredoxin fold that catalyzes disulfide bond formation and isomerization. [provided by RefSeq, Apr 2017]
View all TXNDC15 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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