Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10947563
FKBP5
0.925 0.040 6 35685660 intron variant G/A snv 0.77 3
rs56372821
EPHX2 ; GULOP
1.000 0.080 8 27578983 intron variant G/A snv 0.13 2
rs9316235
HTR2A
13 46871568 intron variant G/A snv 0.19 2
rs110402
CRHR1 ; LINC02210-CRHR1 ; MAPT-AS1
0.790 0.120 17 45802681 intron variant G/A;C snv 12
rs1800532
TPH1
0.763 0.160 11 18026269 intron variant G/T snv 0.33 15
rs893290
RORA
15 61190958 intron variant G/T snv 0.96 1
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs698
ADH1C ; ADH1B
0.724 0.240 4 99339632 missense variant T/A;C snv 0.35 20
rs9470080
FKBP5
0.827 0.080 6 35678658 intron variant T/A;C snv 13
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs3804099
TLR2
0.627 0.680 4 153703504 synonymous variant T/C snv 0.40 0.48 40
rs279858
GABRA2
0.851 0.080 4 46312576 synonymous variant T/C snv 0.40 0.38 8
rs4537731 1.000 0.040 11 18047335 upstream gene variant T/C snv 0.48 3
rs13438494
PCLO
1.000 0.040 7 82759398 intron variant T/G snv 0.61 6