Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs846111
rs846111
1 6219310 missense variant G/C snv 0.24 0.20
QT interval feature (observable entity)
0.800 1.000 4 2009 2019
dbSNP: rs709209
rs709209
1 6218354 missense variant A/G snv 0.35 0.44
QT interval feature (observable entity)
0.700 1.000 1 2009 2009