Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
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
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31 23
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs9296158
FKBP5 ; LOC112267956
0.763 0.080 6 35599305 intron variant A/G snv 0.65 16
rs1800532
TPH1
0.763 0.160 11 18026269 intron variant G/T snv 0.33 15
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
rs4713916
FKBP5
0.790 0.160 6 35702206 intron variant A/C;G;T snv 11
rs737865
TXNRD2 ; COMT
0.763 0.240 22 19942598 intron variant A/G snv 0.23 11
rs7997012
HTR2A
0.807 0.080 13 46837850 intron variant A/G snv 0.69 11
rs10748842
NRG3
0.807 0.120 10 81889983 intron variant T/C snv 0.13 8
rs1535255
CNR1
0.807 0.120 6 88151489 intron variant T/G snv 0.21 8
rs7973260
KSR2
0.851 0.120 12 117937681 intron variant A/G snv 0.83 7
rs10514299
TMEM161B-AS1
0.827 0.120 5 88367793 intron variant C/T snv 0.21 6
rs1545843
LOC107984536
0.827 0.120 12 84170289 intron variant G/A snv 0.52 6
rs2253206 0.851 0.080 2 207527254 intron variant A/G snv 0.47 6
rs3760138
AANAT
0.807 0.160 17 76467027 intron variant G/A;T snv 6
rs11904814
CREB1
0.851 0.080 2 207562074 intron variant T/G snv 0.30 5