rs191648835
This is a intron variant variant in the CFAP299 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.
balding measurement, androgenetic alopecia
Jiang L et al. “A generalized linear mixed model association tool for biobank-scale data.” Nature Genetics 53(11):1616-1621 (2021)
Allele G
OR 0.38
p 3.0e-12
N 207,036
Large GWAS
European
About CFAP299
Predicted to be located in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
View all CFAP299 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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