rs5753179
This is a intron variant variant in the SEC14L6 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.
protein measurement
Pietzner M et al. “Mapping the proteo-genomic convergence of human diseases.” Science (new York, N.y.) 374(6569):eabj1541 (2021)
Allele T
OR 0.14
p 3.0e-25
N 10,708
Large GWAS
European
About SEC14L6
Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
View all SEC14L6 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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