Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs587777308
GABRA1
0.763 0.040 5 161873196 missense variant G/A snv 14
rs587777057
GNAO1
0.827 0.040 16 56336744 missense variant G/A snv 8
rs1060499553
GABRA1
0.827 0.040 5 161890983 missense variant G/A snv 6
rs773171451
KCNQ2 ; LOC105372724
0.882 0.040 20 63413535 missense variant G/A;T snv 8.0E-06 5
rs121917918
SCN1A ; SCN1A-AS1
0.851 0.040 2 166058651 missense variant C/A;T snv 4
rs121917935
SCN1A ; SCN1A-AS1
0.851 0.040 2 166054660 missense variant C/A;T snv 4
rs794726775
SCN1A-AS1 ; SCN1A
0.882 0.040 2 166039420 splice region variant T/A snv 4
rs796052491
GABRA1
0.851 0.040 5 161890982 missense variant T/A;C snv 4
rs796052493
GABRA1
0.851 0.040 5 161895668 missense variant G/A;T snv 4
rs796053361
STXBP1
0.925 0.040 9 127668160 missense variant G/A;T snv 4
rs1057516097
KCNQ2
0.882 0.040 20 63439671 missense variant G/T snv 3
rs118192194
KCNQ2 ; KCNQ2-AS1
0.882 0.040 20 63446769 missense variant G/A snv 3
rs118192226
KCNQ2
0.925 0.040 20 63415086 stop gained G/A;T snv 4.2E-06 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
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
rs886041339
KCNQ2
0.925 0.040 20 63424195 frameshift variant G/-;GG delins 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