LTF, lactotransferrin, 4057

N. diseases: 37; N. variants: 8
Source: CURATED ×
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12629300
rs12629300
Entrez Id: 4057
Gene Symbol: LTF
LTF
CUI: C0149745
Disease:
Oral Ulcer
T 0.700 GeneticVariation GWASCAT Genome wide analysis for mouth ulcers identifies associations at immune regulatory loci. 30837455 2019
dbSNP: rs1126477
rs1126477
Entrez Id: 4057
Gene Symbol: LTF
LTF
CUI: C2985280
Disease:
Blood Protein Measurement
C 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
dbSNP: rs1126477
rs1126477
Entrez Id: 4057
Gene Symbol: LTF
LTF
CUI: C2985280
Disease:
Blood Protein Measurement
T 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs4682816
rs4682816
Entrez Id: 4057
Gene Symbol: LTF
LTF
CUI: C2985280
Disease:
Blood Protein Measurement
G 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs4683234
rs4683234
Entrez Id: 4057
Gene Symbol: LTF
LTF
CUI: C2985280
Disease:
Blood Protein Measurement
G 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs61740470
rs61740470
Entrez Id: 4057
Gene Symbol: LTF
LTF
CUI: C2985280
Disease:
Blood Protein Measurement
T 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs6441996
rs6441996
Entrez Id: 4057
Gene Symbol: LTF
LTF
CUI: C2985280
Disease:
Blood Protein Measurement
C 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs72622926
rs72622926
Entrez Id: 4057
Gene Symbol: LTF
LTF
CUI: C2985280
Disease:
Blood Protein Measurement
C 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs1126478
rs1126478
Entrez Id: 4057
Gene Symbol: LTF
LTF
CUI: C0201850
Disease:
Alkaline phosphatase measurement
C 0.700 GeneticVariation GWASCAT Connecting genetic risk to disease end points through the human blood plasma proteome. 28240269 2017