Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10919019
rs10919019
LINC00970
1.000 0.040 1 168926275 intron variant T/A;C snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs114101204
rs114101204
LINC00970
1 169056816 intron variant G/A snv 1.3E-02
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		0.700 1.000 1 2012 2012
dbSNP: rs114964168
rs114964168
LINC00970
1 169063639 intron variant C/T snv 1.3E-02
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		0.700 1.000 1 2012 2012
dbSNP: rs17514217
rs17514217
LINC00970
1.000 0.040 1 168920169 intron variant T/A snv 9.6E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs17514245
rs17514245
LINC00970
1.000 0.040 1 168920319 intron variant A/G snv 0.10
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs6427160
rs6427160
LINC00970
1.000 0.040 1 168922943 intron variant T/C snv 0.37
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs7530207
rs7530207
LINC00970
1.000 0.040 1 168921182 intron variant G/C snv 0.12
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs78516619
rs78516619
LINC00970
1 168920135 intron variant A/G snv 7.8E-03
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.700 1.000 1 2019 2019
dbSNP: rs911892
rs911892
LINC00970
1.000 0.040 1 168922386 intron variant A/C snv 0.86
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs973608
rs973608
LINC00970
1.000 0.040 1 168919708 intron variant C/T snv 0.13
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs2146204
rs2146204
LINC00970
1 168904861 intron variant A/C snv 0.13
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2012 2012