Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs1800497
ANKK1
0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs1800955
DRD4
0.827 0.160 11 636784 upstream gene variant T/C;G snv 8
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs2023239
CNR1
0.724 0.160 6 88150763 intron variant T/C snv 0.21 20
rs2030324
BDNF
0.827 0.120 11 27705368 intron variant A/G snv 0.49 6
rs2044081
GABRB1
1.000 0.080 4 47216323 intron variant C/T snv 0.14 2
rs2110267
DPP6
1.000 0.040 7 153838604 intergenic variant C/G snv 0.32 3
rs2161961
GNAL
18 11774501 intron variant A/G snv 0.31 3
rs2236225
MTHFD1
0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 52
rs2261722
PCSK5
9 76254665 intron variant G/A snv 0.30 1
rs2284411
GRIN2B
1.000 0.040 12 13713238 intron variant C/T snv 0.34 4
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs265981
DRD1
0.925 0.080 5 175443899 5 prime UTR variant A/G;T snv 3
rs27072
SLC6A3
0.807 0.120 5 1394407 3 prime UTR variant C/A;T snv 11
rs324981
NPSR1-AS1 ; NPSR1
0.724 0.320 7 34778501 missense variant A/T snv 0.44 0.47 18
rs3745406
PRKCG
0.851 0.080 19 53891711 missense variant T/A;C snv 4.0E-06; 0.41 6
rs3746544
SNAP25 ; SNAP25-AS1
0.790 0.120 20 10306436 3 prime UTR variant G/T snv 0.68 10
rs402691
PRKCG
19 53888383 intron variant T/C snv 0.39 2
rs4290270
TPH2
0.724 0.320 12 72022455 synonymous variant A/T snv 0.57 0.55 17
rs4532
DRD1
0.827 0.160 5 175443147 5 prime UTR variant C/T snv 0.68 0.72 7
rs4570625
TPH2
0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs4659682
LGALS8
1 236518948 intron variant A/G snv 0.62 1
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249