rs8176759

This is a coding sequence variant variant in the ABO gene.

GWAS Catalog Trait Associations (7)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

Red cell distribution width

Allele G
OR
p 1.0e-111
N 563,352
Large GWAS
multi-ancestry

mean corpuscular hemoglobin concentration

Allele A
OR
p 2.0e-52
N 630,125
Large GWAS
multi-ancestry

granulocyte percentage of myeloid white cells

Allele A
OR 0.06
p 4.0e-14
N 169,545
Large GWAS
European

platelet crit

Allele A
OR 0.05
p 2.0e-10
N 164,339
Large GWAS
European

erythrocyte count

Verma A et al. Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele G
OR 0.10
p 2.0e-18
N 55,750
Major Consortium StudyLarge GWAS
Hispanic or Latin American

About ABO

This gene encodes proteins related to the first discovered blood group system, ABO. Variation in the ABO gene (chromosome 9q34.2) is the basis of the ABO blood group, thus the presence of an allele determines the blood group in an individual. The 'O' blood group is caused by a deletion of guanine-258 near the N-terminus of the protein which results in a frameshift and translation of an almost entirely different protein. Individuals with the A, B, and AB alleles express glycosyltransferase activities that convert the H antigen into the A or B antigen. Other minor alleles have been found for this gene. [provided by RefSeq, Apr 2022]

View all ABO variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

Community Wiki

No community notes yet for this variant. Sign in to start one.

Comments

Sign in to join the discussion.

Loading comments…