Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs4818
COMT ; MIR4761
0.683 0.440 22 19963684 synonymous variant C/G;T snv 0.34 27
rs3745367
RETN
0.827 0.200 19 7669625 intron variant G/A snv 0.39 8
rs1718125
LOC105370032 ; P2RX7
0.851 0.200 12 121155216 intron variant C/T snv 0.15 0.19 6
rs373611092
MIR4761 ; COMT
0.925 0.160 22 19962794 missense variant A/G snv 8.4E-05 4.9E-05 5
rs3845446
CACNA1E
1 181797301 intron variant T/C snv 6.3E-02 3
rs13080116
SCN11A
3 38865732 intron variant T/C snv 0.23 2
rs33985936
SCN11A
3 38894643 missense variant C/A;T snv 8.0E-06; 0.22 2
rs4286289
SCN9A ; SCN1A-AS1
1.000 0.120 2 166305201 intron variant C/A snv 0.74 2
rs3732765
MED12L ; P2RY12
3 151372636 missense variant G/A snv 0.31 0.28 1
rs795484
TAOK3
12 118152057 intron variant T/C snv 0.71 1