rs1145656
This is a intron variant variant in the FAM168A 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.
heel bone mineral density
Morris JA et al. “An atlas of genetic influences on osteoporosis in humans and mice.” Nature Genetics 51(2):258-266 (2019)
Allele C
OR 0.01
p 3.0e-9
N 426,824
Large GWAS
European
venous thromboembolism
Thibord F et al. “Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors.” Circulation 146(16):1225-1242 (2022)
Allele A
OR 0.04
p 2.0e-8
N 1,066,917
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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