rs12019136

This is a intron variant variant in the FUT6 gene.

GWAS Catalog Trait Associations (9)

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

N-glycan measurement

Allele A
OR 1.11
p 4.0e-167
N 10,172
Large GWAS
European

vitamin B12 measurement

Allele A
OR 0.18
p 2.0e-54
N 38,000
Large GWAS
South Asian

alpha-(1;3)-fucosyltransferase 5 measurement

Allele A
OR 0.76
p 4.0e-50
N 2,935
Large GWAS
Greater Middle Eastern (Middle Eastern, North African or Persian)

lactoperoxidase measurement

Allele A
OR 0.72
p 1.0e-44
N 2,935
Large GWAS
Greater Middle Eastern (Middle Eastern, North African or Persian)

interleukin-18 receptor 1 measurement

Allele A
OR 0.06
p 5.0e-26
N 47,745
Large GWAS
European

cathepsin L2 measurement

Allele A
OR 0.11
p 5.0e-20
N 47,745
Large GWAS
European

E-selectin amount

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 1.0e-14
N 10,708
Large GWAS
European

serum IgG glycosylation measurement

Allele A
OR
p 2.0e-13
N 1,960
Large GWAS
European

transferrin glycosylation measurement

Landini A et al. Genetic regulation of post-translational modification of two distinct proteins. Nature Communications 13(1):1586 (2022)
Allele A
OR 0.84
p 2.0e-22
N 1,890
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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