rs61990092
This is a intron variant variant in the TC2N gene.
▶GWAS Catalog Trait Associations (1)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (1)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
venous thromboembolism
Thibord F et al. “Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors.” Circulation 146(16):1225-1242 (2022)
Allele T
OR 0.06
p 4.0e-21
N 1,066,917
Large GWAS
European
About TC2N
Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
View all TC2N variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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