Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1473473
TPH2
0.925 0.080 12 72010598 intron variant C/A;T snv 0.81 4
rs591556
TPH1
11 18039853 intron variant T/C snv 0.78 1
rs4532
DRD1
0.827 0.160 5 175443147 5 prime UTR variant C/T snv 0.68 0.72 7
rs13212041
LOC105377864 ; HTR1B
0.851 0.200 6 77461407 downstream gene variant C/T snv 0.70 6
rs1455858
LOC349160 ; CHRM2
0.925 0.080 7 136946956 intron variant T/C snv 0.69 3
rs3746544
SNAP25 ; SNAP25-AS1
0.790 0.120 20 10306436 3 prime UTR variant G/T snv 0.68 10
rs4659682
LGALS8
1 236518948 intron variant A/G snv 0.62 1
rs4290270
TPH2
0.724 0.320 12 72022455 synonymous variant A/T snv 0.57 0.55 17
rs1386483
TPH2
0.790 0.080 12 72018714 intron variant T/C snv 0.53 9
rs2030324
BDNF
0.827 0.120 11 27705368 intron variant A/G snv 0.49 6
rs324981
NPSR1-AS1 ; NPSR1
0.724 0.320 7 34778501 missense variant A/T snv 0.44 0.47 18
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs6311
HTR2A
0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs6313
HTR2A
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs402691
PRKCG
19 53888383 intron variant T/C snv 0.39 2
rs2236225
MTHFD1
0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 52
rs6277
DRD2
0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs478597
NOS1
1.000 0.040 12 117313620 intron variant G/A snv 0.35 2
rs2284411
GRIN2B
1.000 0.040 12 13713238 intron variant C/T snv 0.34 4
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
rs2261722
PCSK5
9 76254665 intron variant G/A snv 0.30 1
rs4570625
TPH2
0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs11178999
TPH2
12 71939790 intron variant G/A snv 0.27 1
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174