Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9829896
KAT2B ; MIR3135A
3 20135980 intron variant C/A;T snv 2
rs9470080
FKBP5
0.827 0.080 6 35678658 intron variant T/A;C snv 13
rs9316235
HTR2A
13 46871568 intron variant G/A snv 0.19 2
rs893924483
BDNF ; BDNF-AS
0.716 0.280 11 27658285 missense variant C/A;T snv 4.0E-06 1.4E-05 23
rs893290
RORA
15 61190958 intron variant G/T snv 0.96 1
rs7997012
HTR2A
0.807 0.080 13 46837850 intron variant A/G snv 0.69 11
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs746682028
BDNF ; BDNF-AS
0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs7305115
TPH2
0.807 0.200 12 71979082 synonymous variant A/C;G;T snv 4.0E-06; 0.56 8
rs7044343
LOC107987046 ; IL33
0.752 0.520 9 6254208 intron variant C/T snv 0.51 13
rs698
ADH1C ; ADH1B
0.724 0.240 4 99339632 missense variant T/A;C snv 0.35 20
rs678849
OPRD1
0.882 0.120 1 28818676 intron variant C/T snv 0.44 5
rs6313
HTR2A
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs6311
HTR2A
0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs56372821
EPHX2 ; GULOP
1.000 0.080 8 27578983 intron variant G/A snv 0.13 2
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs4722999
CRHR2
0.851 0.080 7 30654159 intron variant C/T snv 0.67 5
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs4675690 2 207643083 intergenic variant C/T snv 0.48 3
rs4537731 1.000 0.040 11 18047335 upstream gene variant T/C snv 0.48 3
rs3804099
TLR2
0.627 0.680 4 153703504 synonymous variant T/C snv 0.40 0.48 40
rs3798347
FKBP5 ; LOC112267956
0.925 0.040 6 35633999 intron variant A/T snv 0.65 3
rs324420
FAAH
0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs279858
GABRA2
0.851 0.080 4 46312576 synonymous variant T/C snv 0.40 0.38 8