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: rs1553920379
rs1553920379
0.776 0.160 4 101032294 frameshift variant -/AGTA delins
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.700 0
dbSNP: rs1555850842
rs1555850842
1.000 0.040 20 63407136 frameshift variant -/G delins
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.700 0
dbSNP: rs1057519542
rs1057519542
1.000 0.040 X 18604372 frameshift variant -/GACC delins
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.700 0
dbSNP: rs1057518759
rs1057518759
1.000 0.040 X 18604394 frameshift variant -/GC delins
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.700 0
dbSNP: rs796053335
rs796053335
1.000 0.040 9 128632280 protein altering variant -/GCATGC delins
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.700 0
dbSNP: rs786200962
rs786200962
0.827 0.120 19 13298768 frameshift variant A/- del
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.700 1.000 1 2015 2015
dbSNP: rs1569017337
rs1569017337
1.000 0.040 20 49374703 frameshift variant A/- del
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.700 0
dbSNP: rs1554208945
rs1554208945
0.752 0.240 6 87260207 missense variant A/C snv
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.700 0
dbSNP: rs1057519540
rs1057519540
0.925 0.160 12 51768895 missense variant A/G snv
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.700 0
dbSNP: rs1553567473
rs1553567473
0.925 0.040 2 165309193 missense variant A/G snv
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.700 0
dbSNP: rs1555889108
rs1555889108
0.925 0.040 20 49374559 missense variant A/G snv
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.700 0
dbSNP: rs1569017174
rs1569017174
1.000 0.040 20 49374455 missense variant A/G snv
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.700 0
dbSNP: rs796052957
rs796052957
0.925 0.040 2 166054735 missense variant A/G snv
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.700 0
dbSNP: rs1555703272
rs1555703272
0.925 0.080 17 81715568 stop gained A/T snv
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.700 1.000 1 2018 2018
dbSNP: rs1057519536
rs1057519536
0.925 0.040 20 63442424 missense variant A/T snv
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.700 0
dbSNP: rs1553525325
rs1553525325
0.807 0.120 2 166002716 missense variant A/T snv
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.700 0
dbSNP: rs796053083
rs796053083
1.000 0.040 2 165994177 frameshift variant AA/-;A delins
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.700 0
dbSNP: rs1057519538
rs1057519538
1.000 0.040 9 127651622 inframe deletion AAA/- del
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.700 0
dbSNP: rs794726754
rs794726754
0.925 0.040 2 165992262 frameshift variant ACAA/- delins
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.700 0
dbSNP: rs1135401734
rs1135401734
1.000 0.040 1 244855505 frameshift variant AG/- del
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.700 1.000 1 2017 2017
dbSNP: rs1569219844
rs1569219844
1.000 0.040 X 18604845 frameshift variant AG/- del
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.700 0
dbSNP: rs786204967
rs786204967
1.000 0.040 X 18604169 frameshift variant AG/- delins
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.700 0
dbSNP: rs879253748
rs879253748
0.882 0.040 5 161897251 frameshift variant C/- del
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.700 0
dbSNP: rs1569017205
rs1569017205
1.000 0.040 20 49374515 missense variant C/A snv
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.700 0
dbSNP: rs1057519535
rs1057519535
0.925 0.040 20 63439652 missense variant C/A;G snv
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.700 0