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
dbSNP: rs12731646
rs12731646 		1 169121422 intron variant C/T snv 0.31
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs145163454
rs145163454 		1 169121510 intron variant T/C snv 1.6E-02
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		Cardiovascular Diseases 0.700 1.000 1 2019 2019
dbSNP: rs1892094
rs1892094 		1.000 0.040 1 169125221 intron variant C/T snv 0.41
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs75112989
rs75112989 		1 169129899 intron variant G/A snv 5.0E-02
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		Cardiovascular Diseases 0.700 1.000 1 2012 2012
dbSNP: rs77977611
rs77977611 		1 169112554 intron variant T/G snv 3.0E-02
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		Cardiovascular Diseases 0.700 1.000 1 2012 2012
dbSNP: rs2982468
rs2982468 		1 169121733 intron variant T/A snv 7.5E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.010 1.000 1 2009 2009