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: 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: 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: rs121918681
rs121918681
Entrez Id: 7018;100129696
Gene Symbol: TF;INHCAP
TF;INHCAP
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: rs121918681
rs121918681
Entrez Id: 7018;100129696
Gene Symbol: TF;INHCAP
TF;INHCAP
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: rs121918681
rs121918681
Entrez Id: 7018;100129696
Gene Symbol: TF;INHCAP
TF;INHCAP
CUI: C0521802
Disease:
Congenital atransferrinemia 		A 0.800 CausalMutation CLINVAR
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: rs1799852
rs1799852
Entrez Id: 7018
Gene Symbol: TF
TF
CUI: C1304746
Disease:
RDW - Red blood cell distribution width result 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1799852
rs1799852
Entrez Id: 7018
Gene Symbol: TF
TF
CUI: C0427460
Disease:
Red cell distribution width determination 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs6762719
rs6762719
Entrez Id: 7018
Gene Symbol: TF
TF
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs8177247
rs8177247
Entrez Id: 7018
Gene Symbol: TF
TF
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs4854760
rs4854760
Entrez Id: 7018
Gene Symbol: TF
TF
CUI: C2985280
Disease:
Blood Protein Measurement 		A 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
dbSNP: rs8177297
rs8177297
Entrez Id: 7018
Gene Symbol: TF
TF
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs9843728
rs9843728
Entrez Id: 7018;58477
Gene Symbol: TF;SRPRB
TF;SRPRB
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
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: 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: 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