TBL2, transducin beta like 2, 26608

N. diseases: 190; N. variants: 10
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17145738
rs17145738
Entrez Id: 26608
Gene Symbol: TBL2
TBL2
CUI: C0020557
Disease:
Hypertriglyceridemia 		0.710 GeneticVariation BEFREE Variants more frequently identified in isolated hypertriglyceridemias were rs7412 in APOE and rs1800795 in IL6; rs2808607 in CYP7A1 and rs3812316 and rs17145738 in MLXIPL were more frequent in FCHL. 25176936 2014
dbSNP: rs17145738
rs17145738
Entrez Id: 26608
Gene Symbol: TBL2
TBL2
CUI: C0020474
Disease:
Hyperlipidemia, Familial Combined 		0.010 GeneticVariation BEFREE Variants more frequently identified in isolated hypertriglyceridemias were rs7412 in APOE and rs1800795 in IL6; rs2808607 in CYP7A1 and rs3812316 and rs17145738 in MLXIPL were more frequent in FCHL. 25176936 2014
dbSNP: rs17145738
rs17145738
Entrez Id: 26608
Gene Symbol: TBL2
TBL2
CUI: C0020557
Disease:
Hypertriglyceridemia 		C 0.710 GeneticVariation GWASCAT A common variant association study in ethnic Saudi Arabs reveals novel susceptibility loci for hypertriglyceridemia. 27599772 2017
dbSNP: rs17145738
rs17145738
Entrez Id: 26608
Gene Symbol: TBL2
TBL2
CUI: C0202236
Disease:
Triglycerides measurement 		T 0.800 GeneticVariation GWASCAT Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels. 28334899 2017
dbSNP: rs17145738
rs17145738
Entrez Id: 26608
Gene Symbol: TBL2
TBL2
CUI: C0202117
Disease:
Low density lipoprotein cholesterol measurement 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs17145738
rs17145738
Entrez Id: 26608
Gene Symbol: TBL2
TBL2
CUI: C0392885
Disease:
High density lipoprotein measurement 		C 0.800 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018
dbSNP: rs17145738
rs17145738
Entrez Id: 26608
Gene Symbol: TBL2
TBL2
CUI: C0202236
Disease:
Triglycerides measurement 		C 0.800 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018
dbSNP: rs17145738
rs17145738
Entrez Id: 26608
Gene Symbol: TBL2
TBL2
CUI: C0202236
Disease:
Triglycerides measurement 		T 0.800 GeneticVariation GWASCAT Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. 30926973 2019
dbSNP: rs17145738
rs17145738
Entrez Id: 26608
Gene Symbol: TBL2
TBL2
CUI: C0392885
Disease:
High density lipoprotein measurement 		T 0.800 GeneticVariation GWASCAT Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. 30926973 2019
dbSNP: rs17145738
rs17145738
Entrez Id: 26608
Gene Symbol: TBL2
TBL2
CUI: C0202236
Disease:
Triglycerides measurement 		0.800 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
dbSNP: rs2286276
rs2286276
Entrez Id: 26608
Gene Symbol: TBL2
TBL2
CUI: C0202236
Disease:
Triglycerides measurement 		0.800 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
dbSNP: rs17145738
rs17145738
Entrez Id: 26608
Gene Symbol: TBL2
TBL2
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		T 0.700 GeneticVariation GWASCAT Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels. 31578528 2019