rs35033748
This is a upstream gene variant variant in the FAM222B 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.
mean corpuscular hemoglobin
Sakaue S et al. “A cross-population atlas of genetic associations for 220 human phenotypes.” Nature Genetics 53(10):1415-1424 (2021)
Allele C
OR 0.05
p 6.0e-112
N 478,500
Large GWAS
multi-ancestry
Red cell distribution width
Astle WJ et al. “The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.” Cell 167(5):1415-1429.e19 (2016)
Allele C
OR 0.08
p 2.0e-70
N 171,529
Large GWAS
European
About FAM222B
Located in nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
View all FAM222B variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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