Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1562927768
KMT2E
0.790 0.080 7 105101476 frameshift variant AAAGA/- delins 15
rs587777308
GABRA1
0.763 0.040 5 161873196 missense variant G/A snv 14
rs387907281
ATP1A3
0.752 0.280 19 41970284 missense variant C/T snv 13
rs536289169
GSTM1 ; GSTM2
0.752 0.360 1 109688180 missense variant C/T snv 4.8E-04 13
rs1057910
CYP2C9
0.776 0.280 10 94981296 missense variant A/C;G snv 6.3E-02; 4.0E-06 12
rs121908225
CACNA1A
0.790 0.120 19 13365448 missense variant G/A snv 12
rs759317757
OTUD6B
0.807 0.280 8 91078416 frameshift variant TTAAC/- delins 12
rs1057520918
CACNA1A
0.790 0.160 19 13262780 missense variant C/T snv 11
rs386675647
UGT2B7
0.790 0.240 4 69098619 missense variant AT/TC mnv 10
rs796052676
KCNQ3
0.807 0.200 8 132180246 missense variant G/A snv 10
rs1064797103
OTUD6B
0.827 0.280 8 91078597 missense variant A/G snv 9
rs118192211
KCNQ2
0.790 0.080 20 63439644 missense variant G/A;C snv 9
rs121918622
SCN1A-AS1 ; LOC102724058 ; SCN1A
0.790 0.080 2 165992332 missense variant C/A;T snv 4.0E-06 9
rs28934904
MECP2
0.776 0.200 X 154031431 missense variant G/A;C;T snv 9
rs763000109
TNF
0.827 0.240 6 31575788 missense variant C/G;T snv 4.1E-06; 1.6E-05 9
rs796051881
PEX5
0.807 0.440 12 7202274 frameshift variant -/A delins 9
rs1057516085
KCNQ2
0.827 0.080 20 63444747 missense variant C/T snv 8
rs121909674
GABRG2
0.790 0.080 5 162153132 stop gained C/T snv 8
rs1285524167
ABCC8
0.807 0.280 11 17475004 missense variant C/T snv 8.0E-06 8
rs1554823375
WDR37
0.851 0.160 10 1080454 missense variant C/T snv 8
rs28933383
KCNA1
0.851 0.120 12 4912055 missense variant C/A;G;T snv 8
rs398122887
ATP1A3
0.790 0.280 19 41967744 missense variant C/G;T snv 8
rs587777057
GNAO1
0.827 0.040 16 56336744 missense variant G/A snv 8
rs628031
SLC22A1
0.807 0.280 6 160139813 missense variant A/C;G snv 5.3E-05; 0.63 8
rs74315390
KCNQ2
0.790 0.120 20 63439609 missense variant C/G;T snv 8