Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2284147
rs2284147
Entrez Id: 7392
Gene Symbol: USF2
USF2
CUI: C0869220
Disease:
Adverse effects, not elsewhere classified 		A 0.700 GeneticVariation GWASCAT Genetic variation in the Estonian population: pharmacogenomics study of adverse drug effects using electronic health records. 30420678 2019
dbSNP: rs34805185
rs34805185
Entrez Id: 7392
Gene Symbol: USF2
USF2
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs10424619
rs10424619
Entrez Id: 7392
Gene Symbol: USF2
USF2
CUI: C1304746
Disease:
RDW - Red blood cell distribution width result 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs10424619
rs10424619
Entrez Id: 7392
Gene Symbol: USF2
USF2
CUI: C0427460
Disease:
Red cell distribution width determination 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs12973672
rs12973672
Entrez Id: 7392
Gene Symbol: USF2
USF2
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs12973672
rs12973672
Entrez Id: 7392
Gene Symbol: USF2
USF2
CUI: C0524587
Disease:
Mean Corpuscular Volume (result) 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs916145
rs916145
Entrez Id: 7392
Gene Symbol: USF2
USF2
CUI: C0005411
Disease:
Biliary Atresia 		0.010 GeneticVariation BEFREE The study demonstrates that C allele of rs916145 in USF2 gene has more frequency for developing BA, and decreased USF2 protein nuclear translocation might partly play a role in the decreased hepcidin expression in the cholestatic liver injury of the late stage of BA. 18970934 2008
dbSNP: rs916145
rs916145
Entrez Id: 7392
Gene Symbol: USF2
USF2
CUI: C4520983
Disease:
Congenital atresia of extrahepatic bile duct 		0.010 GeneticVariation BEFREE The study demonstrates that C allele of rs916145 in USF2 gene has more frequency for developing BA, and decreased USF2 protein nuclear translocation might partly play a role in the decreased hepcidin expression in the cholestatic liver injury of the late stage of BA. 18970934 2008