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: rs794727444
rs794727444
0.925 0.040 2 165389451 missense variant G/A;T snv
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: rs796053083
rs796053083
1.000 0.040 2 165994177 frameshift variant AA/-;A delins
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: rs1057519529
rs1057519529
1.000 0.040 2 166043864 missense variant C/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: rs267608501
rs267608501
0.882 0.160 X 18587986 missense variant C/T snv
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: 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: rs1569219844
rs1569219844
1.000 0.040 X 18604845 frameshift variant AG/- del
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.700 0
dbSNP: rs1057518928
rs1057518928
1.000 0.040 12 23665471 missense variant G/A snv
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: rs1135401733
rs1135401733
1.000 0.040 1 244856757 stop gained G/A snv
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.700 1.000 1 2017 2017
dbSNP: rs1135401732
rs1135401732
1.000 0.040 1 244859303 stop gained C/A;G;T snv 4.0E-06
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.700 1.000 1 2017 2017
dbSNP: rs779453109
rs779453109
1.000 0.040 1 244863648 frameshift variant GCCTTCCGCC/- delins 1.2E-05 2.8E-05
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.700 1.000 1 2017 2017
dbSNP: rs1057519549
rs1057519549
0.925 0.040 15 26567655 missense variant G/A snv
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.700 0
dbSNP: rs1057519550
rs1057519550
0.925 0.040 15 26621403 missense variant T/G snv
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.700 0
dbSNP: rs747824231
rs747824231
0.882 0.040 6 31782361 missense variant C/G;T snv 4.1E-06
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.700 0
dbSNP: rs763777257
rs763777257
0.882 0.040 6 31785269 stop gained G/A snv 4.0E-06
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.700 0
dbSNP: rs1057519545
rs1057519545
1.000 0.040 6 33435225 missense variant G/C snv
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.700 0
dbSNP: rs775162839
rs775162839
1.000 0.040 4 39505705 missense variant C/T snv 4.8E-05 5.6E-05
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.700 1.000 1 2020 2020
dbSNP: rs536000212
rs536000212
1.000 0.040 1 39854050 frameshift variant G/- delins 3.2E-04
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.700 0
dbSNP: rs1057519547
rs1057519547
0.925 0.040 5 45396550 missense variant C/T snv
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.700 0
dbSNP: rs1057519548
rs1057519548
0.925 0.040 5 45645575 missense variant C/G snv
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.700 0