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
rs28933979
TTR
0.587 0.600 18 31592974 missense variant G/A;C snv 1.0E-04 70
rs6277
DRD2
0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs121918457
PTPN11
0.701 0.280 12 112488466 missense variant C/T snv 4.0E-06 7.0E-06 24
rs6746030
SCN1A-AS1 ; SCN9A
0.763 0.320 2 166242648 missense variant A/G snv 0.88 0.88 16
rs8065080
TRPV1
0.827 0.200 17 3577153 missense variant T/C snv 0.37 0.32 11
rs1800866
SIGMAR1
0.851 0.080 9 34637693 missense variant T/G snv 0.20 0.18 8
rs6796803 0.925 0.040 3 186746318 intron variant T/A;C snv 4
rs4775319
RORA
0.925 0.040 15 60921365 intron variant G/A snv 0.62 4
rs10950641
SNX8
0.925 0.040 7 2294751 intron variant G/A snv 2.9E-02 4
rs104894851
GLA ; RPL36A-HNRNPH2
0.925 0.200 X 101398920 stop gained G/T snv 3
rs104894852
GLA ; RPL36A-HNRNPH2
0.925 0.200 X 101397871 missense variant T/C snv 3
rs4804217
PCP2
1.000 0.040 19 7634461 intron variant C/T snv 0.29 3
rs1017715903
MPZ
1.000 0.080 1 161306854 stop gained C/T snv 2
rs10814130
SIGMAR1
9 34637994 upstream gene variant C/A snv 0.17 1