rs2071699

This is a variant in the FUT1 gene that changes a alanine to an valine.

GWAS Catalog Trait Associations (6)

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

protein FAM3D measurement

Allele A
OR 0.14
p 3.0e-18
N 47,745
Large GWAS
European

interleukin 19 measurement

Allele A
OR 0.17
p 6.0e-17
N 47,745
Large GWAS
European

alkaline phosphatase measurement

Sinnott-Armstrong N et al. Genetics of 35 blood and urine biomarkers in the UK Biobank. Nature Genetics 53(2):185-194 (2021)
Allele A
OR 0.07
p 2.0e-13
N 355,891
Major Consortium StudyLarge GWAS
multi-ancestry

level of cadherin-17 in blood serum

Allele A
OR 0.13
p 1.0e-12
N 47,745
Large GWAS
European

cadherin-1 measurement

Allele A
OR 0.14
p 1.0e-11
N 47,745
Large GWAS
European

ClinVar annotation

Likely Benign
1 submitter

FUT1-related disorder

View on ClinVar →

About FUT1

This gene encodes a Golgi stack membrane protein that is involved in the creation of a precursor of the H antigen, which is required for the final step in the synthesis of soluble A and B antigens. This is one of two genes encoding the galactoside 2-L-fucosyltransferase enzyme. Mutations in this gene are a cause of the H-Bombay blood group. [provided by RefSeq, Aug 2016]

View all FUT1 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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