TF, transferrin, 7018

N. diseases: 47; N. variants: 70
Source: CURATED ×
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1049296
rs1049296
Entrez Id: 7018
Gene Symbol: TF
TF
CUI: C0001948
Disease:
Alcohol consumption 		T 0.800 GeneticVariation GWASDB Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. 21665994 2011
dbSNP: rs1049296
rs1049296
Entrez Id: 7018
Gene Symbol: TF
TF
CUI: C0001948
Disease:
Alcohol consumption 		T 0.800 GeneticVariation GWASCAT Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. 21665994 2011
dbSNP: rs121918679
rs121918679
Entrez Id: 7018
Gene Symbol: TF
TF
CUI: C0521802
Disease:
Congenital atransferrinemia 		0.800 GeneticVariation UNIPROT Molecular characterization of a third case of human atransferrinemia. 15466165 2004
dbSNP: rs121918679
rs121918679
Entrez Id: 7018
Gene Symbol: TF
TF
CUI: C0521802
Disease:
Congenital atransferrinemia 		0.800 GeneticVariation UNIPROT Molecular characterization of a case of atransferrinemia. 11110675 2000
dbSNP: rs121918679
rs121918679
Entrez Id: 7018
Gene Symbol: TF
TF
CUI: C0521802
Disease:
Congenital atransferrinemia 		C 0.800 CausalMutation CLINVAR
dbSNP: rs1799899
rs1799899
Entrez Id: 7018
Gene Symbol: TF
TF
CUI: C0001948
Disease:
Alcohol consumption 		A 0.800 GeneticVariation GWASDB Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. 21665994 2011
dbSNP: rs1799899
rs1799899
Entrez Id: 7018
Gene Symbol: TF
TF
CUI: C0001948
Disease:
Alcohol consumption 		A 0.800 GeneticVariation GWASCAT Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. 21665994 2011
dbSNP: rs3811647
rs3811647
Entrez Id: 7018
Gene Symbol: TF
TF
CUI: C0001948
Disease:
Alcohol consumption 		A 0.800 GeneticVariation GWASDB Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. 21665994 2011
dbSNP: rs3811647
rs3811647
Entrez Id: 7018
Gene Symbol: TF
TF
CUI: C0001948
Disease:
Alcohol consumption 		A 0.800 GeneticVariation GWASCAT Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. 21665994 2011
dbSNP: rs3811647
rs3811647
Entrez Id: 7018
Gene Symbol: TF
TF
CUI: C0392514
Disease:
Hereditary hemochromatosis 		0.710 GeneticVariation GWASCAT Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis. 25457201 2015
dbSNP: rs1049296
rs1049296
Entrez Id: 7018
Gene Symbol: TF
TF
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: rs1115219
rs1115219
Entrez Id: 7018
Gene Symbol: TF
TF
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: rs1115219
rs1115219
Entrez Id: 7018
Gene Symbol: TF
TF
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: rs121918676
rs121918676
Entrez Id: 7018
Gene Symbol: TF
TF
CUI: C3889615
Disease:
TRANSFERRIN VARIANT D1 PHENOTYPE 		A 0.700 CausalMutation CLINVAR
dbSNP: rs121918677
rs121918677
Entrez Id: 7018
Gene Symbol: TF
TF
CUI: C3889617
Disease:
TRANSFERRIN VARIANT B2 PHENOTYPE 		A 0.700 CausalMutation CLINVAR
dbSNP: rs121918678
rs121918678
Entrez Id: 7018
Gene Symbol: TF
TF
CUI: C3889619
Disease:
TRANSFERRIN VARIANT Bv PHENOTYPE 		G 0.700 CausalMutation CLINVAR
dbSNP: rs121918680
rs121918680
Entrez Id: 7018
Gene Symbol: TF
TF
CUI: C0521802
Disease:
Congenital atransferrinemia 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1358022
rs1358022
Entrez Id: 7018
Gene Symbol: TF
TF
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: rs1358023
rs1358023
Entrez Id: 7018
Gene Symbol: TF
TF
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs1358024
rs1358024
Entrez Id: 7018
Gene Symbol: TF
TF
CUI: C0001948
Disease:
Alcohol consumption 		0.700 GeneticVariation GWASDB Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. 21665994 2011
dbSNP: rs150854910
rs150854910
Entrez Id: 7018
Gene Symbol: TF
TF
CUI: C0524587
Disease:
Mean Corpuscular Volume (result) 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs150854910
rs150854910
Entrez Id: 7018
Gene Symbol: TF
TF
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs1525889
rs1525889
Entrez Id: 7018
Gene Symbol: TF
TF
CUI: C0001948
Disease:
Alcohol consumption 		0.700 GeneticVariation GWASDB Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. 21665994 2011
dbSNP: rs1525892
rs1525892
Entrez Id: 7018
Gene Symbol: TF
TF
CUI: C0001948
Disease:
Alcohol consumption 		0.700 GeneticVariation GWASDB Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. 21665994 2011
dbSNP: rs1525892
rs1525892
Entrez Id: 7018
Gene Symbol: TF
TF
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