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
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs3800373
LOC101929309 ; FKBP5
0.752 0.200 6 35574699 3 prime UTR variant C/A snv 0.68 22
rs10767664
BDNF
0.752 0.400 11 27704439 intron variant T/A snv 0.83 16
rs821616
DISC1 ; TSNAX-DISC1
0.752 0.200 1 232008852 missense variant A/T snv 0.26 0.29 13
rs12273363
BDNF
0.807 0.120 11 27723312 intron variant T/C snv 0.16 11
rs2682826
NOS1
0.807 0.280 12 117215033 3 prime UTR variant G/A snv 0.25 11
rs734312
WFS1
0.790 0.240 4 6301627 missense variant G/A snv 0.55 0.42 10
rs7124442
BDNF-AS ; BDNF
0.827 0.160 11 27655494 3 prime UTR variant C/G;T snv 9
rs908867 0.851 0.160 11 27724217 intron variant C/G;T snv 7
rs1491850 0.925 0.080 11 27728178 intron variant T/C snv 0.37 6
rs10868235
NTRK2
0.925 0.040 9 84878840 intron variant C/T snv 0.40 6
rs4307059 0.882 0.080 5 25967594 intron variant T/A;C snv 5
rs6943555
AUTS2
0.882 0.080 7 70341037 intron variant T/A snv 0.34 5
rs1491851 0.925 0.080 11 27731216 intron variant T/C;G snv 0.41 4
rs962369
BDNF
11 27712873 intron variant T/C snv 0.24 3
rs1800042
HTR1A
1.000 0.040 5 63960902 missense variant C/A;T snv 8.0E-06; 1.4E-03 2
rs121908538
SUCLA2
1.000 13 47954510 missense variant G/A snv 3.2E-05 1.4E-05 2