rs2724564
This is a intron variant variant in the FHIP1A 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.
platelet count
Chen MH et al. “Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.” Cell 182(5):1198-1213.e14 (2020)
Allele T
OR 0.03
p 6.0e-46
N 542,827
Large GWAS
European
Kachuri L et al. “Genetic determinants of blood-cell traits influence susceptibility to childhood acute lymphoblastic leukemia.” American Journal of Human Genetics 108(10):1823-1835 (2021)
Allele T
OR —
p 3.0e-16
N 235,256
Large GWAS
European
About FHIP1A
Involved in protein localization to perinuclear region of cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
View all FHIP1A variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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