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
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs6280
DRD3
0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs6746030
SCN1A-AS1 ; SCN9A
0.763 0.320 2 166242648 missense variant A/G snv 0.88 0.88 16
rs8007267 0.882 0.200 14 54912273 intergenic variant C/T snv 0.31 6
rs3783641
GCH1
0.882 0.120 14 54893421 intron variant T/A;C snv 0.25 4
rs10483639 1.000 0.040 14 54839739 downstream gene variant G/C snv 0.26 3
rs13361160 1.000 0.040 5 10169711 downstream gene variant T/C snv 0.34 2
rs563649
OPRM1
1.000 0.040 6 154086832 5 prime UTR variant C/T snv 9.8E-02 2
rs6476030
DOCK8
1.000 0.040 9 289061 intron variant A/G snv 7.1E-02 1
rs12584920
HTR2A
1.000 0.040 13 46890902 intron variant G/C;T snv 1
rs1777971
LOC101927293
1.000 0.040 6 58143645 intron variant A/G;T snv 1