rs78060698

This is a regulatory region variant variant in the FUT6 gene.

GWAS Catalog Trait Associations (7)

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

N-glycan measurement

Allele A
OR 1.14
p 2.0e-124
N 7,540
Large GWAS
multi-ancestry

transcobalamin-1 measurement

Allele A
OR 0.19
p 3.0e-53
N 47,745
Large GWAS
European

level of folate receptor alpha in blood

Allele A
OR 0.17
p 2.0e-41
N 47,745
Large GWAS
European

galactoside 3(4)-L-fucosyltransferase measurement

Allele A
OR 0.78
p 4.0e-39
N 2,935
Large GWAS
Greater Middle Eastern (Middle Eastern, North African or Persian)

galectin-3 measurement

Allele A
OR 0.06
p 2.0e-36
N 47,745
Large GWAS
European
Pietzner M et al. Mapping the proteo-genomic convergence of human diseases. Science (new York, N.y.) 374(6569):eabj1541 (2021)
Allele A
OR 0.25
p 2.0e-15
N 10,708
Large GWAS
European

alkaline phosphatase measurement

Allele G
OR 0.00
p 1.0e-15
N 437,438
Large GWAS
European

About FUT6

The protein encoded by this gene is a Golgi stack membrane protein that is involved in the creation of sialyl-Lewis X, an E-selectin ligand. Mutations in this gene are a cause of fucosyltransferase-6 deficiency. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]

View all FUT6 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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