Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs4938723
MIR34C ; BTG4 ; MIR34B ; LOC728196
0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
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
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs2254298
CAV3 ; OXTR
0.701 0.200 3 8760542 intron variant G/A snv 0.16 23
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31 23
rs2023239
CNR1
0.724 0.160 6 88150763 intron variant T/C snv 0.21 20
rs9296158
FKBP5 ; LOC112267956
0.763 0.080 6 35599305 intron variant A/G snv 0.65 16
rs9470080
FKBP5
0.827 0.080 6 35678658 intron variant T/A;C snv 13
rs10994336
ANK3
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 12
rs2710102
CNTNAP2
0.790 0.120 7 147877298 intron variant A/G;T snv 12
rs2066713
SLC6A4
0.807 0.200 17 30224647 intron variant G/A snv 0.34 9
rs2535629
ITIH3
0.827 0.040 3 52799203 intron variant G/A;C snv 9
rs2069845
IL6
0.807 0.120 7 22730530 intron variant G/A snv 0.61 8
rs4251417
SLC6A4
0.827 0.200 17 30224840 intron variant C/T snv 6.8E-02 7
rs1018381
DTNBP1
0.882 0.040 6 15656839 intron variant G/A snv 0.16 6
rs13438494
PCLO
1.000 0.040 7 82759398 intron variant T/G snv 0.61 6
rs7341475
RELN
0.851 0.240 7 103764368 intron variant G/A snv 0.17 6
rs736707
LOC101927870 ; RELN
0.851 0.040 7 103489956 intron variant A/G snv 0.30 6
rs2279709
SLC18A1
0.882 0.120 8 20178722 intron variant T/G snv 0.51 5
rs279871
GABRA2
0.882 0.080 4 46303716 intron variant T/C snv 0.38 5
rs40184
SLC6A3
0.851 0.120 5 1394962 intron variant C/T snv 0.45 5