Disease: Mental Depression
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs324420
FAAH
0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31 23
rs1800497
ANKK1
0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs1043307
PSMD9
0.776 0.360 12 121915890 missense variant A/C;G snv 14
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs6314
HTR2A
0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02 23
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs334558
LOC107986119 ; GSK3B
0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51 20
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs5522
NR3C2
0.732 0.320 4 148436323 missense variant C/T snv 0.88 0.89 19
rs1801260
CLOCK ; TMEM165
0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs2230912
P2RX7 ; LOC105370032
0.752 0.280 12 121184393 missense variant A/G snv 0.13 0.12 16
rs5569
SLC6A2
0.742 0.280 16 55697923 synonymous variant G/A;C snv 0.31; 4.0E-06 19
rs6937506 0.807 0.280 6 132578260 intergenic variant G/A snv 0.25 7
rs1176744
HTR3B
0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 19
rs749437638
ARVCF ; COMT
0.752 0.240 22 19968597 missense variant C/T snv 2.4E-05 1.4E-05 14
rs1805054
HTR6
0.708 0.200 1 19666020 synonymous variant C/T snv 0.15; 8.0E-06 0.16 17
rs2227631
SERPINE1
0.742 0.200 7 101126257 upstream gene variant A/G snv 0.54 13
rs242941
MAPT-AS1 ; CRHR1 ; LINC02210-CRHR1
0.790 0.200 17 45815154 intron variant A/C snv 0.62 9
rs3093077 0.827 0.200 1 159709846 upstream gene variant A/C;G;T snv 9
rs3800373
LOC101929309 ; FKBP5
0.752 0.200 6 35574699 3 prime UTR variant C/A snv 0.68 22
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs7305115
TPH2
0.807 0.200 12 71979082 synonymous variant A/C;G;T snv 4.0E-06; 0.56 8