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: rs6038724
rs6038724 		20 7149091 intron variant T/C snv 0.28
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2009 2009
dbSNP: rs6038725
rs6038725 		20 7152392 intron variant A/G;T snv
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2009 2009
dbSNP: rs6038726
rs6038726 		20 7155675 intron variant C/G;T snv
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2009 2009
dbSNP: rs6038727
rs6038727 		20 7155710 intron variant C/G snv 0.31
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2009 2009
dbSNP: rs6038729
rs6038729 		20 7157110 intron variant A/C;T snv
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2009 2009
dbSNP: rs6054768
rs6054768 		20 7149030 intron variant C/T snv 0.28
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2009 2009
dbSNP: rs6054770
rs6054770 		20 7151105 intron variant G/A snv 0.35
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2009 2009
dbSNP: rs6054771
rs6054771 		20 7151563 intron variant T/C snv 0.28
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2009 2009
dbSNP: rs6054776
rs6054776 		20 7155369 intron variant G/C;T snv
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2009 2009
dbSNP: rs6054777
rs6054777 		20 7155597 intron variant G/A snv 0.31
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2009 2009
dbSNP: rs6107933
rs6107933 		20 7151869 intron variant G/A;T snv
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2009 2009
dbSNP: rs6117650
rs6117650 		20 7154986 intron variant G/A;T snv
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2009 2009
dbSNP: rs719563
rs719563 		20 7162350 intron variant G/A snv 0.42
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2009 2009