rs7183988

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

GWAS Catalog Trait Associations (7)

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

coronary artery disease

Allele T
OR 1.06
p 3.0e-33
N 1,165,690
Large GWAS
European, NR

Beta blocking 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 G
OR 0.07
p 6.0e-24
N 402,750
Large GWAS
multi-ancestry
Allele G
OR 0.08
p 4.0e-21
N 224,024
Major Consortium StudyLarge GWAS
European

birth weight, parental genotype effect measurement

Allele G
OR 0.03
p 1.0e-20
N 230,069
Large GWAS
European

neutrophil count

Allele G
OR 0.02
p 6.0e-18
N 519,288
Large GWAS
European

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 G
OR 0.07
p 2.0e-14
N 630,096
Large GWAS
multi-ancestry

brain connectivity attribute

Allele T
OR 5.67
p 1.0e-8
N 30,810
Large GWAS
European

insomnia measurement

Allele G
OR 1.04
p 2.0e-8
N 1,331,010
Large GWAS
European

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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