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: rs11866328
rs11866328
0.925 0.120 16 9768699 intron variant G/T snv 0.38
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
Digestive System Diseases; Infections 0.810 1.000 1 2011 2011
dbSNP: rs397518447
rs397518447
0.925 0.040 16 9829585 missense variant G/T snv
EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION
0.800 1.000 13 2010 2017
dbSNP: rs397518470
rs397518470
1.000 16 9840745 missense variant C/A;T snv
EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION
0.800 1.000 13 2010 2017
dbSNP: rs762659685
rs762659685
1.000 16 9822286 missense variant C/T snv
EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION
0.800 1.000 13 2010 2017
dbSNP: rs397514557
rs397514557
1.000 16 9829485 missense variant G/C snv
EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION
0.800 1.000 12 2010 2017
dbSNP: rs397518450
rs397518450
1.000 16 9834227 missense variant G/C snv
EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION
0.800 1.000 12 2010 2017
dbSNP: rs397518471
rs397518471
1.000 16 9829476 missense variant A/C snv
EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION
0.800 1.000 12 2010 2017
dbSNP: rs1250662891
rs1250662891
0.925 0.040 16 10180176 missense variant G/C snv 4.0E-06
EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION
0.700 1.000 12 2010 2017
dbSNP: rs1360906241
rs1360906241
1.000 16 9840788 missense variant G/A snv
EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION
0.700 1.000 12 2010 2017
dbSNP: rs1555482933
rs1555482933
0.925 0.040 16 9764834 missense variant T/A snv
EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION
0.700 1.000 12 2010 2017
dbSNP: rs1555488144
rs1555488144
0.925 0.040 16 9798454 missense variant C/T snv
EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION
0.700 1.000 12 2010 2017
dbSNP: rs1555491648
rs1555491648
0.925 0.040 16 9822337 missense variant G/A snv
EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION
0.700 1.000 12 2010 2017
dbSNP: rs1555496111
rs1555496111
0.925 0.040 16 9849778 missense variant A/G snv
EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION
0.700 1.000 12 2010 2017
dbSNP: rs199528312
rs199528312
1.000 16 9938097 missense variant G/A snv 3.6E-05 1.4E-05
EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION
0.700 1.000 12 2010 2017
dbSNP: rs397518468
rs397518468
1.000 16 9840706 missense variant G/A snv
EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION
0.700 1.000 12 2010 2017
dbSNP: rs886039239
rs886039239
1.000 16 9764617 missense variant T/C snv 8.0E-06
EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION
0.700 1.000 12 2010 2017
dbSNP: rs933322445
rs933322445
1.000 16 9764747 missense variant C/T snv
EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION
0.700 1.000 12 2010 2017
dbSNP: rs397518465
rs397518465
0.925 0.040 16 9937958 splice donor variant C/A;T snv
EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION
0.700 1.000 4 2013 2017
dbSNP: rs9922678
rs9922678
1.000 0.040 16 9852462 intron variant G/A;C snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 4 2014 2019
dbSNP: rs7191183
rs7191183
1.000 0.040 16 9806200 intron variant T/C snv 0.35
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 3 2017 2019
dbSNP: rs11074547
rs11074547
16 10043032 intron variant T/G snv 0.32
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 1 2019 2019
dbSNP: rs11647445
rs11647445
0.925 0.040 16 9833109 intron variant T/G snv 0.35
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs11647445
rs11647445
0.925 0.040 16 9833109 intron variant T/G snv 0.35
CUI: C0236773
Disease: Depressed bipolar I disorder
Depressed bipolar I disorder
Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs117304774
rs117304774
1.000 0.040 16 10057377 intron variant G/A snv 8.2E-03
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs117304774
rs117304774
1.000 0.040 16 10057377 intron variant G/A snv 8.2E-03
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019