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: rs10919071
rs10919071 		1 169130245 intron variant A/G snv 0.10
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.800 1.000 2 2009 2019
dbSNP: rs10919070
rs10919070 		1 169129799 intron variant A/C snv 0.10
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 2 2014 2019
dbSNP: rs11809180
rs11809180 		1 169130857 intron variant C/A;T snv
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 2 2014 2019
dbSNP: rs12035622
rs12035622 		1 169133102 intron variant T/A snv 9.9E-02
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 2 2017 2019
dbSNP: rs12079745
rs12079745 		1 169131822 3 prime UTR variant G/A snv 0.10
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 2 2014 2019
dbSNP: rs1138486
rs1138486 		1 169132697 3 prime UTR variant C/G;T snv 0.12
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2017 2017