Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs546151500
ZNF142
0.925 0.080 2 218643341 stop gained G/A;T snv 8.0E-06; 4.0E-06 5
rs34757931
VPS11
0.742 0.360 11 119081189 missense variant T/G snv 1.2E-04 5.6E-05 26
rs864309505
TPP1
0.807 0.200 11 6615220 missense variant T/G snv 10
rs753635972
ST20-MTHFS ; MTHFS
0.790 0.120 15 79845388 missense variant C/T snv 3.2E-05 2.1E-05 15
rs797044927
SCN2A
0.925 0.080 2 165388746 missense variant G/A snv 3
rs121918622
SCN1A-AS1 ; LOC102724058 ; SCN1A
0.790 0.080 2 165992332 missense variant C/A;T snv 4.0E-06 9
rs863225422
RNU4ATAC ; CLASP1 ; LOC107985942
0.742 0.440 2 121530927 non coding transcript exon variant G/A snv 4.6E-05; 7.7E-06 4.9E-05 23
rs1555565492
RAI1
0.776 0.160 17 17795417 frameshift variant -/G delins 18
rs1553920379
PPP3CA
0.776 0.160 4 101032294 frameshift variant -/AGTA delins 27
rs758946412
PCDH19
0.790 0.240 X 100407507 frameshift variant G/-;GG delins 12
rs1569315842
PCDH19
1.000 0.080 X 100408107 frameshift variant -/G delins 1
rs1065852
NDUFA6-DT ; LOC112268294 ; CYP2D6
0.695 0.360 22 42130692 missense variant G/A snv 0.21 0.19 19
rs587777893
MTOR
0.658 0.240 1 11128107 missense variant G/A;T snv 67
rs771379232
MTHFS ; ST20-MTHFS
0.790 0.120 15 79845338 stop gained G/A snv 2.0E-05 3.5E-05 15
rs118192250
KCNQ3
0.851 0.120 8 132175457 missense variant C/A snv 5
rs74315390
KCNQ2
0.790 0.120 20 63439609 missense variant C/G;T snv 8
rs2486253
KCNJ10
0.882 0.080 1 160039629 3 prime UTR variant A/C;T snv 3
rs727502818
KCNC1
0.790 0.160 11 17772053 missense variant G/A snv 26
rs7588807
INHA
0.925 0.080 2 219574380 intron variant G/T snv 0.48 2
rs869312825
GNB1
0.827 0.120 1 1804548 start lost T/C snv 11
rs869312826
GNB1
0.882 0.080 1 1787378 missense variant C/T snv 6
rs112894280
GABRG2
1.000 0.080 5 162093956 missense variant A/G snv 4.0E-06 1.4E-05 1
rs4906902
GABRB3
0.724 0.200 15 26774621 intron variant A/G snv 0.15 14
rs1553798675
FGF12
0.925 0.080 3 192335441 missense variant C/T snv 4
rs137852776
EFHC1
0.827 0.080 6 52452799 missense variant T/C snv 3.5E-03 2.4E-03 5