TF, transferrin, 7018

N. diseases: 168; N. variants: 74
Source: ALL
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 GWASCAT 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 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: 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: 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 BEFREE Because these two outcomes were clearly associated with the biochemical and clinical expression of the disease, an indirect link between the rs3811647 polymorphism and the phenotypic presentation of HFE-HH is likely. 25457201 2015
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: C0427460
Disease:
Red cell distribution width determination 		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: C1304746
Disease:
RDW - Red blood cell distribution width result 		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 		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: 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: 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