FOXI1, forkhead box I1, 2299

N. diseases: 42; N. variants: 9
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10057744
rs10057744
Entrez Id: 2299
Gene Symbol: FOXI1
FOXI1
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: rs10063424
rs10063424
Entrez Id: 2299
Gene Symbol: FOXI1
FOXI1
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: rs11951903
rs11951903
Entrez Id: 2299
Gene Symbol: FOXI1
FOXI1
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs12516022
rs12516022
Entrez Id: 2299
Gene Symbol: FOXI1
FOXI1
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: rs2879269
rs2879269
Entrez Id: 2299
Gene Symbol: FOXI1
FOXI1
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: rs4315935
rs4315935
Entrez Id: 2299
Gene Symbol: FOXI1
FOXI1
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: rs6555888
rs6555888
Entrez Id: 2299
Gene Symbol: FOXI1
FOXI1
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: rs6873124
rs6873124
Entrez Id: 2299
Gene Symbol: FOXI1
FOXI1
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: rs121909341
rs121909341
Entrez Id: 2299
Gene Symbol: FOXI1
FOXI1
CUI: C0271829
Disease:
Pendred's syndrome
A 0.700 CausalMutation CLINVAR
dbSNP: rs121909341
rs121909341
Entrez Id: 2299
Gene Symbol: FOXI1
FOXI1
CUI: C3538946
Disease:
DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT
A 0.700 CausalMutation CLINVAR