rs7952686
This is a intron variant variant in the FAM168A 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.
tumor necrosis factor receptor superfamily member 19L amount
Allele T
OR 0.41
p 3.0e-45
N 3,301
Large GWAS
European
About FAM168A
Involved in positive regulation of base-excision repair. [provided by Alliance of Genome Resources, Jul 2025]
View all FAM168A variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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