rs13289928
This is a intron variant variant in the MYMK 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.
blood group A
Wang M et al. “Genomic Association vs. Serological Determination of ABO Blood Types in a Chinese Cohort, with Application in Mendelian Randomization.” Genes 12(7) (2021)
Allele A
OR 1.80
p 5.0e-8
N 1,008
Large GWAS
East Asian
About MYMK
Involved in myoblast fusion. Located in plasma membrane. Implicated in Carey-Fineman-Ziter syndrome. [provided by Alliance of Genome Resources, Apr 2025]
View all MYMK variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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