RNF207, ring finger protein 207, 388591

N. diseases: 6; N. variants: 3
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs846111
rs846111
Entrez Id: 388591
Gene Symbol: RNF207
RNF207
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: rs846111
rs846111
Entrez Id: 388591
Gene Symbol: RNF207
RNF207
CUI: C0429028
Disease:
QT interval feature (observable entity) 		C 0.800 GeneticVariation GWASCAT Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization. 24952745 2014
dbSNP: rs846111
rs846111
Entrez Id: 388591
Gene Symbol: RNF207
RNF207
CUI: C0429028
Disease:
QT interval feature (observable entity) 		C 0.800 GeneticVariation GWASCAT Common variants at ten loci influence QT interval duration in the QTGEN Study. 19305408 2009
dbSNP: rs846111
rs846111
Entrez Id: 388591
Gene Symbol: RNF207
RNF207
CUI: C0429028
Disease:
QT interval feature (observable entity) 		C 0.800 GeneticVariation GWASDB Common variants at ten loci modulate the QT interval duration in the QTSCD Study. 19305409 2009
dbSNP: rs846111
rs846111
Entrez Id: 388591
Gene Symbol: RNF207
RNF207
CUI: C0429028
Disease:
QT interval feature (observable entity) 		C 0.800 GeneticVariation GWASCAT Common variants at ten loci modulate the QT interval duration in the QTSCD Study. 19305409 2009
dbSNP: rs846111
rs846111
Entrez Id: 388591
Gene Symbol: RNF207
RNF207
CUI: C0429028
Disease:
QT interval feature (observable entity) 		C 0.800 GeneticVariation GWASDB Common variants at ten loci influence QT interval duration in the QTGEN Study. 19305408 2009
dbSNP: rs145358377
rs145358377
Entrez Id: 388591
Gene Symbol: RNF207
RNF207
CUI: C1821417
Disease:
RESTING HEART RATE 		GA 0.700 GeneticVariation GWASCAT Identification of genomic loci associated with resting heart rate and shared genetic predictors with all-cause mortality. 27798624 2016
dbSNP: rs709209
rs709209
Entrez Id: 388591
Gene Symbol: RNF207
RNF207
CUI: C0429028
Disease:
QT interval feature (observable entity) 		0.700 GeneticVariation GWASDB Common variants at ten loci modulate the QT interval duration in the QTSCD Study. 19305409 2009