Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs3789243
ABCB1
0.776 0.120 7 87591570 intron variant A/G snv 0.50 14
rs587777308
GABRA1
0.763 0.040 5 161873196 missense variant G/A snv 14
rs3219151
GABRA6
0.752 0.160 5 161701908 3 prime UTR variant C/T snv 0.51 14
rs4906902
GABRB3
0.724 0.200 15 26774621 intron variant A/G snv 0.15 14
rs211037
GABRG2
0.742 0.240 5 162101274 synonymous variant C/T snv 0.28 0.31 14
rs1130183
KCNJ10
0.827 0.160 1 160041722 missense variant G/A snv 4.6E-02 4.7E-02 6
rs886039373
GABRA1
0.882 0.040 5 161882639 missense variant G/A snv 4
rs2229902
GRM7
0.851 0.160 3 7452730 missense variant A/T snv 0.31 0.30 4
rs1561587715
GABRA1
0.925 0.040 5 161895676 frameshift variant TGCTCACCATGACAACATTG/- delins 3
rs1883415
GPLD1
0.925 0.040 6 24491247 intron variant A/C snv 0.34 3
rs2486253
KCNJ10
0.882 0.080 1 160039629 3 prime UTR variant A/C;T snv 3
rs142740233
SLC12A5
0.925 0.080 20 46056217 missense variant G/A;T snv 3.3E-03; 4.0E-06 3
rs121918771
SCN1A ; SCN1A-AS1
0.925 0.040 2 166051793 missense variant G/A snv 1.2E-05 2.8E-05 2
rs16850331
SCN2A
0.925 0.080 2 165292743 intron variant C/T snv 0.23 2
rs3943809
SCN2A
0.925 0.080 2 165344371 intron variant A/G snv 0.20 2
rs548424453
SLC12A5
1.000 0.040 20 46057189 missense variant C/A;T snv 5.2E-05 2
rs635311
SLC4A3
0.925 0.040 2 219637645 missense variant A/C;T snv 0.75; 8.0E-06 2
rs41307846
GABRD
1.000 0.040 1 2028260 missense variant G/A snv 1.7E-02 1.7E-02 1
rs1801475
KCNQ2
1.000 0.040 20 63406924 missense variant T/G snv 0.61 0.59 1
rs1801545
KCNQ2
1.000 0.040 20 63414925 synonymous variant G/A;C;T snv 9.3E-05; 7.2E-02 1
rs796053048
LOC102724058 ; SCN1A-AS1 ; SCN1A
1.000 0.040 2 165991522 missense variant G/A snv 1
rs1559144583
SCN1A-AS1 ; LOC102724058 ; SCN1A
1.000 0.040 2 166012137 stop gained C/T snv 1