SLC4A4, solute carrier family 4 member 4, 8671

N. diseases: 58; N. variants: 11
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: rs2579330
rs2579330
Entrez Id: 8671
Gene Symbol: SLC4A4
SLC4A4
CUI: C0429028
Disease:
QT interval feature (observable entity) 		C 0.800 GeneticVariation GWASDB Impact of ancestry and common genetic variants on QT interval in African Americans. 23166209 2012
dbSNP: rs2579330
rs2579330
Entrez Id: 8671
Gene Symbol: SLC4A4
SLC4A4
CUI: C0429028
Disease:
QT interval feature (observable entity) 		C 0.800 GeneticVariation GWASCAT Impact of ancestry and common genetic variants on QT interval in African Americans. 23166209 2012