SLC19A2, solute carrier family 19 member 2, 10560

N. diseases: 70; N. variants: 15
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: rs1983546
rs1983546
Entrez Id: 10560
Gene Symbol: SLC19A2
SLC19A2
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: rs1983546
rs1983546
Entrez Id: 10560
Gene Symbol: SLC19A2
SLC19A2
CUI: C0429028
Disease:
QT interval feature (observable entity) 		G 0.700 GeneticVariation GWASCAT Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization. 24952745 2014