NME7, NME/NM23 family member 7, 29922

N. diseases: 28; N. variants: 14
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: rs16861990
rs16861990 		1 169165889 intron variant A/C snv 5.5E-02
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		Cardiovascular Diseases 0.800 1.000 2 2011 2012
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: rs1208327
rs1208327 		1 169327626 intron variant C/G;T snv
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		Cardiovascular Diseases 0.700 1.000 2 2011 2012
dbSNP: rs10800427
rs10800427 		1 169303213 non coding transcript exon variant A/C;T snv 0.96
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		Cardiovascular Diseases 0.700 1.000 1 2012 2012
dbSNP: rs10800428
rs10800428 		1 169303215 non coding transcript exon variant G/A;T snv 0.96
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		Cardiovascular Diseases 0.700 1.000 1 2012 2012
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: rs1200063
rs1200063 		1 169345192 intron variant T/C snv 0.95
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		Cardiovascular Diseases 0.700 1.000 1 2012 2012
dbSNP: rs1208327
rs1208327 		1 169327626 intron variant C/G;T snv
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		Cardiovascular Diseases 0.700 1.000 1 2012 2012
dbSNP: rs1209731
rs1209731 		1 169355555 intron variant T/C;G snv
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		Cardiovascular Diseases 0.700 1.000 1 2012 2012
dbSNP: rs1209731
rs1209731 		1 169355555 intron variant T/C;G snv
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		Cardiovascular Diseases 0.700 1.000 1 2019 2019
dbSNP: rs12753816
rs12753816 		1.000 0.040 1 169183350 intron variant C/T snv 0.24
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs144737447
rs144737447 		1 169191220 intron variant C/T snv 1.7E-02
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		Cardiovascular Diseases 0.700 1.000 1 2012 2012
dbSNP: rs16861990
rs16861990 		1 169165889 intron variant A/C snv 5.5E-02
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		Cardiovascular Diseases 0.700 1.000 1 2012 2012
dbSNP: rs2040445
rs2040445 		1 169247174 intron variant C/G;T snv
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		Cardiovascular Diseases 0.700 1.000 1 2019 2019
dbSNP: rs2179490
rs2179490 		1 169140155 intron variant G/A snv 0.33
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs2227246
rs2227246 		1 169238941 intron variant C/T snv 0.98
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		Cardiovascular Diseases 0.700 1.000 1 2012 2012
dbSNP: rs77979353
rs77979353 		1 169145784 intron variant T/C snv 3.4E-02
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		Cardiovascular Diseases 0.700 1.000 1 2012 2012