rs6465867
This is a intron variant variant in the PHTF2 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.
atrial fibrillation
Jordà P et al. “Genetic analyses across cardiovascular traits: leveraging genetic correlations to empower locus discovery and prediction in common cardiovascular diseases.” Npj Genomic Medicine 10(1):65 (2025)
Allele C
OR 5.57
p 3.0e-8
N 296,021
Large GWAS
European
About PHTF2
Located in endoplasmic reticulum. [provided by Alliance of Genome Resources, Jul 2025]
View all PHTF2 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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