FOXF2, forkhead box F2, 2295

N. diseases: 57; N. variants: 2
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs199564443
rs199564443
Entrez Id: 2295;105374880
Gene Symbol: FOXF2;LOC105374880
FOXF2;LOC105374880
CUI: C0272178
Disease:
Drug-induced neutropenia
0.700 GeneticVariation GWASCAT Three SNPs were strongly associated with antithyroid drug-induced agranulocytosis: rs652888 (OR 4·73, 95% CI 3·00-7·44, p=1·92 × 10(-11)) and rs199564443 (17·42, 7·38-41·12, p=7·04 × 10(-11)), which were independent of HLA-B*27:05, and rs1071816 (5·27, 3·06-9·10, p=2·35 × 10(-9)) which was in moderate linkage disequilibrium with HLA-B*27:05. 27157822 2016
dbSNP: rs1711972
rs1711972
Entrez Id: 2295;105374880
Gene Symbol: FOXF2;LOC105374880
FOXF2;LOC105374880
CUI: C0948008
Disease:
Ischemic stroke
0.010 GeneticVariation BEFREE By the genotype analysis, a novel SNP rs1711972, near <i>FOXF2</i>, was observed to be associated with an increased risk of ischemic stroke(CA genotype, adjusted OR = 1.35; 95% CI, 1.07 to 1.70), but not significantly after Bonferroni corrections for multiple tests. 29163794 2017
dbSNP: rs1711972
rs1711972
Entrez Id: 2295;105374880
Gene Symbol: FOXF2;LOC105374880
FOXF2;LOC105374880
CUI: C0038454
Disease:
Cerebrovascular accident
0.010 GeneticVariation BEFREE However, in the subgroup analysis, we discovered that rs1711972 was associated with an increased risk of large-artery atherosclerotic stroke in the additive model (<i>P</i> = 0.020; CA genotype, adjusted OR = 1.50; 95%CI, 1.09 to 2.07) and dominant model (<i>P</i> = 0.010; OR = 1.47; 95%CI, 1.09 to 1.99). 29163794 2017
dbSNP: rs1711972
rs1711972
Entrez Id: 2295;105374880
Gene Symbol: FOXF2;LOC105374880
FOXF2;LOC105374880
CUI: C0007131
Disease:
Non-Small Cell Lung Carcinoma
0.010 GeneticVariation BEFREE FOXF2 rs1711972A>C and HEYL rs784621G>A were associated with survival outcomes of surgically treated NSCLC. 28766235 2017