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
rs324420
FAAH
0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs8065080
TRPV1
0.827 0.200 17 3577153 missense variant T/C snv 0.37 0.32 11
rs920829
MSC-AS1 ; TRPA1
0.925 0.160 8 72065468 missense variant C/T snv 0.14 0.16 3
rs748409227
ANK1
8 41708865 synonymous variant C/T snv 1.6E-05 7.0E-06 2
rs745525088
ANK1
8 41714203 missense variant C/G;T snv 4.8E-06; 2.4E-05 1