Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4675690 2 207643083 intergenic variant C/T snv 0.48 3
rs1885884
HTR2A ; HTR2A-AS1
13 46856141 non coding transcript exon variant C/A;G;T snv 2
rs9316235
HTR2A
13 46871568 intron variant G/A snv 0.19 2
rs9829896
KAT2B ; MIR3135A
3 20135980 intron variant C/A;T snv 2
rs893290
RORA
15 61190958 intron variant G/T snv 0.96 1
rs13438494
PCLO
1.000 0.040 7 82759398 intron variant T/G snv 0.61 6
rs10947563
FKBP5
0.925 0.040 6 35685660 intron variant G/A snv 0.77 3
rs12701020
CRHR2
0.925 0.040 7 30655345 intron variant C/T snv 0.12 3
rs3798347
FKBP5 ; LOC112267956
0.925 0.040 6 35633999 intron variant A/T snv 0.65 3
rs4537731 1.000 0.040 11 18047335 upstream gene variant T/C snv 0.48 3
rs9470080
FKBP5
0.827 0.080 6 35678658 intron variant T/A;C snv 13
rs7997012
HTR2A
0.807 0.080 13 46837850 intron variant A/G snv 0.69 11
rs279858
GABRA2
0.851 0.080 4 46312576 synonymous variant T/C snv 0.40 0.38 8
rs4722999
CRHR2
0.851 0.080 7 30654159 intron variant C/T snv 0.67 5
rs1800498
DRD2
0.882 0.080 11 113420866 intron variant G/A snv 0.44 4
rs279826
GABRA2
1.000 0.080 4 46332192 intron variant A/G snv 0.46 4
rs56372821
EPHX2 ; GULOP
1.000 0.080 8 27578983 intron variant G/A snv 0.13 2
rs110402
CRHR1 ; LINC02210-CRHR1 ; MAPT-AS1
0.790 0.120 17 45802681 intron variant G/A;C snv 12
rs678849
OPRD1
0.882 0.120 1 28818676 intron variant C/T snv 0.44 5
rs1800532
TPH1
0.763 0.160 11 18026269 intron variant G/T snv 0.33 15
rs7305115
TPH2
0.807 0.200 12 71979082 synonymous variant A/C;G;T snv 4.0E-06; 0.56 8
rs698
ADH1C ; ADH1B
0.724 0.240 4 99339632 missense variant T/A;C snv 0.35 20
rs893924483
BDNF ; BDNF-AS
0.716 0.280 11 27658285 missense variant C/A;T snv 4.0E-06 1.4E-05 23
rs11792633
IL33 ; LOC107987046
0.882 0.280 9 6248035 intron variant C/T snv 0.35 5
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42