rs4318720, LINC02263

N. diseases: 1
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
QT interval feature (observable entity)
CUI: C0429028
Disease: QT interval feature (observable entity)
226 4 117411099 non coding transcript exon variant G/A snv 0.12 0.800 1.000 1 2009 2009