Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3219151
GABRA6
0.752 0.160 5 161701908 3 prime UTR variant C/T snv 0.51 14
rs3789243
ABCB1
0.776 0.120 7 87591570 intron variant A/G snv 0.50 14
rs4906902
GABRB3
0.724 0.200 15 26774621 intron variant A/G snv 0.15 14
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
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
rs694539
NNMT
0.776 0.200 11 114262697 intron variant C/T snv 0.21 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
rs28934904
MECP2
0.776 0.200 X 154031431 missense variant G/A;C;T snv 9
rs4523957
SMG6 ; SRR
0.790 0.120 17 2305605 intron variant G/T snv 0.54 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
rs10818488
C5-OT1
0.776 0.360 9 120942809 regulatory region variant A/G snv 0.51 8
rs121909674
GABRG2
0.790 0.080 5 162153132 stop gained C/T snv 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
rs3755724
TIMP4 ; SYN2
0.790 0.360 3 12159406 intron variant C/T snv 0.31 8
rs3761847
TRAF1
0.827 0.200 9 120927961 intron variant G/A snv 0.52 8
rs3812718
SCN1A-AS1 ; SCN1A
0.776 0.240 2 166053034 splice region variant C/T snv 0.48 8
rs398122887
ATP1A3
0.790 0.280 19 41967744 missense variant C/G;T snv 8