FETUB, fetuin B, 26998

N. diseases: 38; N. variants: 7
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs72625023
rs72625023
Entrez Id: 26998;105374258
Gene Symbol: FETUB;LOC105374258
FETUB;LOC105374258
CUI: C2985280
Disease:
Blood Protein Measurement
T 0.700 GeneticVariation GWASCAT Genome and epigenome wide studies of neurological protein biomarkers in the Lothian Birth Cohort 1936. 31320639 2019
dbSNP: rs11719860
rs11719860
Entrez Id: 26998;105374258
Gene Symbol: FETUB;LOC105374258
FETUB;LOC105374258
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: rs35530899
rs35530899
Entrez Id: 26998;105374258
Gene Symbol: FETUB;LOC105374258
FETUB;LOC105374258
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: rs3817400
rs3817400
Entrez Id: 26998;105374258
Gene Symbol: FETUB;LOC105374258
FETUB;LOC105374258
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: rs3817400
rs3817400
Entrez Id: 26998;105374258
Gene Symbol: FETUB;LOC105374258
FETUB;LOC105374258
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: rs6767451
rs6767451
Entrez Id: 26998;105374258
Gene Symbol: FETUB;LOC105374258
FETUB;LOC105374258
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: rs7999
rs7999
Entrez Id: 26998;105374258
Gene Symbol: FETUB;LOC105374258
FETUB;LOC105374258
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: rs4686434
rs4686434
Entrez Id: 26998;105374258
Gene Symbol: FETUB;LOC105374258
FETUB;LOC105374258
CUI: C0400966
Disease:
Non-alcoholic Fatty Liver Disease
0.010 GeneticVariation BEFREE Carrying the minor G allele for FETUB rs4686434 was significantly associated with decreased IHTG content and may affect hepatic triglyceride accumulation in individuals at high risk of non-alcoholic fatty liver disease. 29671945 2018