rs1894401

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

GWAS Catalog Trait Associations (8)

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

level of tyrosine-protein kinase Fes/Fps in blood

Allele A
OR 0.13
p 6.0e-94
N 47,745
Large GWAS
European

Diuretic use measurement

Allele G
OR 0.07
p 6.0e-19
N 229,086
Major Consortium StudyLarge GWAS
European
Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele G
OR 0.06
p 2.0e-18
N 407,812
Large GWAS
multi-ancestry

myocardial infarction

Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele A
OR 0.09
p 2.0e-18
N 623,029
Large GWAS
multi-ancestry

neutrophil count

Allele A
OR
p 3.0e-17
N 627,215
Large GWAS
multi-ancestry
Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele A
OR 0.02
p 3.0e-13
N 432,666
Large GWAS
multi-ancestry

angina pectoris

Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele A
OR 0.08
p 1.0e-16
N 508,073
Large GWAS
multi-ancestry

myeloid leukocyte count

Allele A
OR
p 3.0e-16
N 746,667
Large GWAS
multi-ancestry

osteoarthritis

Hatzikotoulas K et al. Translational genomics of osteoarthritis in 1,962,069 individuals. Nature 641(8065):1217-1224 (2025)
Allele A
OR 1.02
p 1.0e-11
N 1,962,069
Large GWAS
multi-ancestry

Antithrombotic agent use measurement

Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele A
OR 0.03
p 3.0e-8
N 332,365
Large GWAS
multi-ancestry

About FES

This gene encodes the human cellular counterpart of a feline sarcoma retrovirus protein with transforming capabilities. The gene product has tyrosine-specific protein kinase activity and that activity is required for maintenance of cellular transformation. Its chromosomal location has linked it to a specific translocation event identified in patients with acute promyelocytic leukemia but it is also involved in normal hematopoiesis as well as growth factor and cytokine receptor signaling. Alternative splicing results in multiple variants encoding different isoforms.[provided by RefSeq, Jan 2009]

View all FES variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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