Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6313
HTR2A
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs324420
FAAH
0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs6311
HTR2A
0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs6277
DRD2
0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs4570625
TPH2
0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs1801028
DRD2
0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02 24
rs1800532
TPH1
0.763 0.160 11 18026269 intron variant G/T snv 0.33 15
rs1317286
CHRNA3
0.925 0.120 15 78603787 intron variant A/G snv 0.30 6
rs604300
MGLL
1.000 0.080 3 127724009 intron variant A/G snv 0.91 3
rs10799590
CNIH3
1 224634780 intron variant G/A snv 0.56 2
rs2619528
DTNBP1
1.000 0.040 6 15649598 intron variant C/T snv 0.26 2
rs1254341668
DTNBP1
6 15523111 missense variant G/A snv 4.0E-06 1
rs1019385
GRIN2B
12 13981909 splice region variant C/A snv 0.37 1