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: rs10482996
rs10482996
21 29492492 intron variant C/T snv 7.6E-02
QT interval feature (observable entity)
0.700 1.000 1 2009 2009
dbSNP: rs2000460
rs2000460
21 29494804 intron variant A/G snv 0.86
QT interval feature (observable entity)
0.700 1.000 1 2009 2009
dbSNP: rs2211887
rs2211887
21 29492828 intron variant T/C snv 0.82
QT interval feature (observable entity)
0.700 1.000 1 2009 2009
dbSNP: rs2832357
rs2832357
21 29491574 intron variant A/G snv 0.12
QT interval feature (observable entity)
0.700 1.000 1 2009 2009
dbSNP: rs2832361
rs2832361
21 29498804 intron variant C/T snv 6.4E-02
QT interval feature (observable entity)
0.700 1.000 1 2009 2009
dbSNP: rs2832367
rs2832367
21 29501649 intron variant C/T snv 8.0E-02
QT interval feature (observable entity)
0.700 1.000 1 2009 2009
dbSNP: rs963072
rs963072
21 29495316 intron variant T/A;C;G snv
QT interval feature (observable entity)
0.700 1.000 1 2009 2009
dbSNP: rs963073
rs963073
21 29495132 intron variant T/C snv 0.83
QT interval feature (observable entity)
0.700 1.000 1 2009 2009
dbSNP: rs980007
rs980007
21 29492962 intron variant A/G snv 0.83
QT interval feature (observable entity)
0.700 1.000 1 2009 2009