rs13335629
This is a intron variant variant in the FAM234A gene.
▶GWAS Catalog Trait Associations (4)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (4)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
mean corpuscular hemoglobin concentration
Chen Z et al. “Genome-wide association analysis of red blood cell traits in African Americans: the COGENT Network.” Human Molecular Genetics 22(12):2529-38 (2013)
Allele A
OR 0.33
p 9.0e-48
N 16,485
Large GWAS
multi-ancestry
hemoglobin measurement
Kowalski MH et al. “Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations.” Plos Genetics 15(12):e1008500 (2019)
Allele A
OR 0.21
p 1.0e-43
N 43,187
Major Consortium StudyLarge GWAS
multi-ancestry
Chen Z et al. “Genome-wide association analysis of red blood cell traits in African Americans: the COGENT Network.” Human Molecular Genetics 22(12):2529-38 (2013)
Allele A
OR 0.19
p 3.0e-23
N 16,485
Large GWAS
multi-ancestry
erythrocyte count
Chen Z et al. “Genome-wide association analysis of red blood cell traits in African Americans: the COGENT Network.” Human Molecular Genetics 22(12):2529-38 (2013)
Allele A
OR 0.17
p 7.0e-24
N 16,485
Large GWAS
multi-ancestry
Hodonsky CJ et al. “Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos.” Plos Genetics 13(4):e1006760 (2017)
Allele A
OR 0.15
p 2.0e-13
N 12,502
Large GWAS
Hispanic or Latin American
erythrocyte volume
Chen Z et al. “Genome-wide association analysis of red blood cell traits in African Americans: the COGENT Network.” Human Molecular Genetics 22(12):2529-38 (2013)
Allele A
OR 0.65
p 4.0e-22
N 16,485
Large GWAS
multi-ancestry
About FAM234A
Located in cell surface. [provided by Alliance of Genome Resources, Jul 2025]
View all FAM234A variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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