Source: CLINVAR

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: rs1568940442
rs1568940442
20 63444765 missense variant G/A snv
CUI: C0036572
Disease: Seizures
Seizures
0.700 1.000 5 2007 2015
dbSNP: rs1555850151
rs1555850151
1.000 20 63406659 frameshift variant -/GCCCA delins
CUI: C0036572
Disease: Seizures
Seizures
0.700 1.000 3 2003 2014
dbSNP: rs1564367605
rs1564367605
9 135768856 missense variant G/A snv
CUI: C0036572
Disease: Seizures
Seizures
0.700 1.000 3 2015 2017
dbSNP: rs796052653
rs796052653
0.925 20 63413526 missense variant C/A;T snv
CUI: C0036572
Disease: Seizures
Seizures
0.700 1.000 3 2013 2015
dbSNP: rs587777219
rs587777219
0.925 20 63442428 missense variant G/A snv
CUI: C0036572
Disease: Seizures
Seizures
0.700 1.000 2 2012 2015
dbSNP: rs1057516032
rs1057516032
1.000 19 41970211 protein altering variant AGTCT/GA delins
CUI: C0036572
Disease: Seizures
Seizures
0.700 1.000 1 2016 2016
dbSNP: rs1554434435
rs1554434435
1.000 7 44284206 stop gained G/A snv
CUI: C0036572
Disease: Seizures
Seizures
0.700 1.000 1 2017 2017
dbSNP: rs797044519
rs797044519
0.925 21 37478285 stop gained C/A;G;T snv
CUI: C0036572
Disease: Seizures
Seizures
0.700 1.000 1 2015 2015
dbSNP: rs797044520
rs797044520
0.925 21 37505442 stop gained C/T snv
CUI: C0036572
Disease: Seizures
Seizures
0.700 1.000 1 2015 2015
dbSNP: rs797044521
rs797044521
0.925 21 37480768 frameshift variant A/- delins
CUI: C0036572
Disease: Seizures
Seizures
0.700 1.000 1 2015 2015
dbSNP: rs797044522
rs797044522
0.925 21 37496119 frameshift variant AGAT/- delins
CUI: C0036572
Disease: Seizures
Seizures
0.700 1.000 1 2015 2015
dbSNP: rs797044523
rs797044523
0.882 21 37480756 frameshift variant -/A delins
CUI: C0036572
Disease: Seizures
Seizures
0.700 1.000 1 2015 2015
dbSNP: rs797044524
rs797044524
0.925 21 37486513 missense variant A/T snv
CUI: C0036572
Disease: Seizures
Seizures
0.700 1.000 1 2015 2015
dbSNP: rs797044525
rs797044525
0.925 21 37490244 missense variant T/G snv
CUI: C0036572
Disease: Seizures
Seizures
0.700 1.000 1 2015 2015
dbSNP: rs797044526
rs797044526
0.925 21 37490393 missense variant C/T snv
CUI: C0036572
Disease: Seizures
Seizures
0.700 1.000 1 2015 2015
dbSNP: rs797044938
rs797044938
20 63442529 missense variant C/A;G snv
CUI: C0036572
Disease: Seizures
Seizures
0.700 1.000 1 2016 2016
dbSNP: rs868732642
rs868732642
4 127938782 splice donor variant C/A;T snv 4.0E-06
CUI: C0036572
Disease: Seizures
Seizures
0.700 1.000 1 2012 2012
dbSNP: rs876661308
rs876661308
1.000 5 88823780 missense variant T/A snv
CUI: C0036572
Disease: Seizures
Seizures
0.700 1.000 1 2016 2016
dbSNP: rs878853280
rs878853280
1.000 9 109137529 stop gained G/A snv
CUI: C0036572
Disease: Seizures
Seizures
0.700 1.000 1 2016 2016
dbSNP: rs878853281
rs878853281
1.000 9 109141360 stop gained C/T snv 4.0E-06
CUI: C0036572
Disease: Seizures
Seizures
0.700 1.000 1 2016 2016
dbSNP: rs878853282
rs878853282
1.000 9 109141466 inframe deletion CCT/- delins 2.0E-05 2.7E-04
CUI: C0036572
Disease: Seizures
Seizures
0.700 1.000 1 2016 2016
dbSNP: rs878853283
rs878853283
1.000 9 109149675 frameshift variant -/T delins
CUI: C0036572
Disease: Seizures
Seizures
0.700 1.000 1 2016 2016
dbSNP: rs1057517891
rs1057517891
15 89333346 stop gained G/A snv
CUI: C0036572
Disease: Seizures
Seizures
0.700 0
dbSNP: rs1057518770
rs1057518770
1.000 15 25354536 missense variant C/T snv
CUI: C0036572
Disease: Seizures
Seizures
0.700 0
dbSNP: rs1057518821
rs1057518821
1.000 1 42930671 frameshift variant -/C delins
CUI: C0036572
Disease: Seizures
Seizures
0.700 0