rs4657178, NOS1AP

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 1 162240820 intron variant C/A;G;T snv 0.31 0.800 1.000 2 2009 2019