Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs138877187
SCN1A-AS1 ; SCN1A
0.882 0.080 2 166045081 stop gained G/A;C;T snv 7.6E-05 3
rs1555869758
KCNQ2
1.000 0.040 20 63438654 missense variant T/C snv 3
rs397514581
KCNQ2
0.882 0.040 20 63444711 missense variant C/T snv 3
rs398122854
ARX
0.882 0.040 X 25015657 stop gained G/C snv 3
rs398123593
SCN1A-AS1 ; LOC102724058 ; SCN1A
0.882 0.040 2 166002537 stop gained G/A snv 3
rs759584387
LOC105372724 ; KCNQ2
0.882 0.040 20 63413556 missense variant G/A;T snv 4.0E-06 3
rs794726730
SCN1A-AS1 ; SCN1A
0.882 0.080 2 166042334 stop gained G/A snv 3
rs794727740
KCNQ2
0.925 0.040 20 63442429 missense variant C/G;T snv 3
rs797045599
GNAO1
0.882 0.040 16 56336817 missense variant C/T snv 3
rs864321707
KCNQ2
0.882 0.040 20 63439608 missense variant G/A snv 3
rs886044717
KCNT1
0.925 0.040 9 135779423 missense variant T/A snv 3
rs1057516098
KCNQ2
0.925 0.040 20 63439657 missense variant C/T snv 2
rs1057523858
SCN1A-AS1 ; SCN1A
0.925 0.040 2 166047647 missense variant A/T snv 2
rs118192215
KCNQ2
0.925 0.040 20 63438651 missense variant G/A snv 2
rs118192228
KCNQ2
0.925 0.040 20 63414902 splice donor variant C/T snv 2
rs121917927
SCN1A-AS1 ; SCN1A
0.925 0.040 2 166046969 missense variant C/G;T snv 2
rs121917969
SCN1A ; SCN1A-AS1
0.925 0.040 2 166037891 missense variant A/G snv 2
rs121918765
SCN1A-AS1 ; SCN1A ; LOC102724058
0.925 0.040 2 165992284 missense variant A/G;T snv 2
rs121918788
SCN1A-AS1 ; SCN1A
0.925 0.040 2 166037931 missense variant G/A snv 2
rs1554965669
SLC25A22
0.925 0.040 11 792888 stop gained G/A snv 2
rs542420576
SCN1A ; SCN1A-AS1 ; LOC102724058
0.925 0.040 2 166036371 stop gained G/A;T snv 4.1E-06 2
rs587777310
STXBP1
0.925 0.040 9 127668132 missense variant G/A snv 2
rs587777420
NECAP1
0.925 0.040 12 8089982 stop gained C/T snv 7.0E-06 2
rs587784453
STXBP1
0.925 0.040 9 127666236 missense variant A/G snv 2
rs727503974
KCNQ2
0.925 0.040 20 63439704 missense variant G/A snv 2