Disease: QT interval feature (observable entity) ×
Source: ALL
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: rs3934467
rs3934467 		1 162212887 intron variant C/T snv 0.27
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.800 1.000 4 2012 2019
dbSNP: rs10494366
rs10494366 		0.851 0.200 1 162115895 intron variant G/T snv 0.54
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.800 1.000 3 2006 2019
dbSNP: rs12029454
rs12029454 		1 162163327 intron variant G/A snv 0.21
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.800 1.000 3 2009 2019
dbSNP: rs16857031
rs16857031 		1 162143120 intron variant C/G snv 0.18
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.800 1.000 3 2009 2019
dbSNP: rs4657175
rs4657175 		1.000 0.040 1 162225948 intron variant T/C;G snv
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.800 1.000 3 2012 2019
dbSNP: rs4657178
rs4657178 		1 162240820 intron variant C/A;G;T snv 0.31
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.800 1.000 2 2009 2019
dbSNP: rs1415259
rs1415259 		0.925 0.080 1 162115519 intron variant C/T snv 0.54
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 2 2010 2019
dbSNP: rs4657172
rs4657172 		1 162209842 intron variant C/G snv 0.82
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 2 2014 2019
dbSNP: rs10127719
rs10127719 		1 162186380 intron variant T/A;C snv
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2012 2012
dbSNP: rs10800352
rs10800352 		1 162202899 intron variant A/G snv 0.27
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2012 2012
dbSNP: rs10918602
rs10918602 		1 162067910 upstream gene variant T/C snv 0.25
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2012 2012
dbSNP: rs12027785
rs12027785 		1 162211355 intron variant T/A snv 0.27
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2012 2012
dbSNP: rs12116744
rs12116744 		1 162210666 intron variant G/A snv 0.27
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2012 2012
dbSNP: rs12123267
rs12123267 		1 162229561 intron variant C/T snv 0.27
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2012 2012
dbSNP: rs12567315
rs12567315 		1 162196856 intron variant G/A snv 0.27
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2012 2012
dbSNP: rs17457880
rs17457880 		1 162198364 intron variant G/A snv 2.0E-02
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2014 2014
dbSNP: rs17460657
rs17460657 		1 162292036 intron variant A/C snv 4.5E-02
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2014 2014
dbSNP: rs347272
rs347272 		1 162348708 intron variant A/G snv 0.82
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2014 2014
dbSNP: rs4306106
rs4306106 		1 162202204 intron variant G/A snv 0.27
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2012 2012
dbSNP: rs4391647
rs4391647 		1 162217141 intron variant A/G snv 0.27
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2012 2012
dbSNP: rs4480335
rs4480335 		1 162203587 intron variant A/C snv 0.27
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2012 2012
dbSNP: rs4657173
rs4657173 		1 162215756 intron variant G/T snv 0.27
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2012 2012
dbSNP: rs6664702
rs6664702 		1 162235117 intron variant T/C snv 0.32
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2012 2012
dbSNP: rs6667431
rs6667431 		1 162198131 intron variant G/A snv 0.27
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2012 2012
dbSNP: rs6692381
rs6692381 		1 162198094 intron variant C/T snv 0.27
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2012 2012