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
rs6313
HTR2A
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs63751273
MAPT
0.645 0.280 17 46010389 missense variant C/T snv 42
rs370717845
HGSNAT
0.763 0.320 8 43161462 missense variant G/A snv 33
rs74315401
PRNP
0.683 0.320 20 4699525 missense variant C/T snv 32
rs1561904557
CSF1R
0.851 0.160 5 150056050 missense variant GGAT/TGCC mnv 9
rs17746510
RAPGEF4
0.882 0.080 2 173019562 intron variant T/C;G snv 5
rs2075572
OPRM1
1.000 0.040 6 154090869 intron variant G/C snv 0.54 2