Disease: Mental Depression
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs10223646
DSE
0.882 0.080 6 116296236 intron variant C/T snv 0.41 4
rs10514299
TMEM161B-AS1
0.827 0.120 5 88367793 intron variant C/T snv 0.21 6
rs1106634
ATP6V1B2
0.851 0.080 8 20208538 intron variant G/A;C;T snv 0.18 5
rs11904814
CREB1
0.851 0.080 2 207562074 intron variant T/G snv 0.30 5
rs12912233
RORA
0.851 0.120 15 60974897 intron variant C/T snv 0.38 5
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs1545843
LOC107984536
0.827 0.120 12 84170289 intron variant G/A snv 0.52 6
rs174697
ARVCF ; COMT
0.851 0.080 22 19966309 intron variant A/G snv 0.88 5
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs2253206 0.851 0.080 2 207527254 intron variant A/G snv 0.47 6
rs242941
MAPT-AS1 ; CRHR1 ; LINC02210-CRHR1
0.790 0.200 17 45815154 intron variant A/C snv 0.62 9
rs2619522
DTNBP1
0.827 0.080 6 15653418 intron variant A/C snv 0.26 6
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31 23
rs4713916
FKBP5
0.790 0.160 6 35702206 intron variant A/C;G;T snv 11
rs528732638
CHST9 ; AQP4-AS1
0.851 0.120 18 26940224 intron variant A/-;AA;AAA;AAAA delins 5
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
rs738499
TEF ; LOC105373042
0.851 0.120 22 41381096 intron variant G/T snv 0.76 9
rs760761
DTNBP1
0.882 0.080 6 15650901 intron variant G/A snv 0.26 4
rs7997012
HTR2A
0.807 0.080 13 46837850 intron variant A/G snv 0.69 11
rs9296158
FKBP5 ; LOC112267956
0.763 0.080 6 35599305 intron variant A/G snv 0.65 16