EPHA6, EPH receptor A6, 285220

N. diseases: 23; N. variants: 9
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1547399
rs1547399
Entrez Id: 285220
Gene Symbol: EPHA6
EPHA6
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs2027815
rs2027815
Entrez Id: 285220
Gene Symbol: EPHA6
EPHA6
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs2213253
rs2213253
Entrez Id: 285220
Gene Symbol: EPHA6
EPHA6
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs2213254
rs2213254
Entrez Id: 285220
Gene Symbol: EPHA6
EPHA6
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs4621347
rs4621347
Entrez Id: 285220
Gene Symbol: EPHA6
EPHA6
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs4857055
rs4857055
Entrez Id: 285220
Gene Symbol: EPHA6
EPHA6
CUI: C0871470
Disease:
Systolic Pressure 		0.700 GeneticVariation GWASCAT In the hypertension group, a significant association was observed between systolic BP and the rs4857055 polymorphism. 29208002 2017
dbSNP: rs9824190
rs9824190
Entrez Id: 285220
Gene Symbol: EPHA6
EPHA6
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs301927
rs301927
Entrez Id: 285220
Gene Symbol: EPHA6
EPHA6
CUI: C0442874
Disease:
Neuropathy 		0.010 GeneticVariation BEFREE Among the seven polymorphisms selected for genotyping, the variant alleles of <i>EPHA5</i>-rs7349683, <i>EPHA6</i>-rs301927, and <i>EPHA8</i>-rs209709 were associated with an increased risk of paclitaxel-induced neuropathy. 31023863 2019
dbSNP: rs4857055
rs4857055
Entrez Id: 285220
Gene Symbol: EPHA6
EPHA6
CUI: C0020538
Disease:
Hypertensive disease 		0.010 GeneticVariation BEFREE These results could suggest that the EPHA6 rs4857055 C > T SNP is a novel candidate gene for hypertension in the Korean population. 29208002 2017
dbSNP: rs7644468
rs7644468
Entrez Id: 285220
Gene Symbol: EPHA6
EPHA6
CUI: C0017168
Disease:
Gastroesophageal reflux disease 		0.010 GeneticVariation BEFREE Four SNPs (PERP rs648802; PIK3CA rs4855094, rs7644468 and TNFRSF1A rs4149579) had significant interaction with gastroesophageal reflux disease (GERD). 21212151 2011