CEP85L, centrosomal protein 85 like, 387119

N. diseases: 40; N. variants: 12
Disease: QT interval feature (observable entity) ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11756438
rs11756438
Entrez Id: 387119
Gene Symbol: CEP85L
CEP85L
CUI: C0429028
Disease:
QT interval feature (observable entity) 		0.800 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
dbSNP: rs11756438
rs11756438
Entrez Id: 387119
Gene Symbol: CEP85L
CEP85L
CUI: C0429028
Disease:
QT interval feature (observable entity) 		A 0.800 GeneticVariation GWASDB Common variants at ten loci influence QT interval duration in the QTGEN Study. 19305408 2009
dbSNP: rs11756438
rs11756438
Entrez Id: 387119
Gene Symbol: CEP85L
CEP85L
CUI: C0429028
Disease:
QT interval feature (observable entity) 		A 0.800 GeneticVariation GWASCAT Common variants at ten loci influence QT interval duration in the QTGEN Study. 19305408 2009
dbSNP: rs11752626
rs11752626
Entrez Id: 387119;105377971
Gene Symbol: CEP85L;LOC105377971
CEP85L;LOC105377971
CUI: C0429028
Disease:
QT interval feature (observable entity) 		0.700 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
dbSNP: rs3902035
rs3902035
Entrez Id: 387119
Gene Symbol: CEP85L
CEP85L
CUI: C0429028
Disease:
QT interval feature (observable entity) 		C 0.700 GeneticVariation GWASCAT Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization. 24952745 2014