Disease: Depressive Symptoms
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs110402
CRHR1 ; LINC02210-CRHR1 ; MAPT-AS1
0.790 0.120 17 45802681 intron variant G/A;C snv 12
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs1799889
SERPINE1
0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs2287161
MTERF2
0.827 0.080 12 106987362 upstream gene variant C/G;T snv 7
rs2535629
ITIH3
0.827 0.040 3 52799203 intron variant G/A;C snv 9
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs6994992
NRG1
0.790 0.120 8 31638065 upstream gene variant C/A;T snv 13
rs7124442
BDNF-AS ; BDNF
0.827 0.160 11 27655494 3 prime UTR variant C/G;T snv 9
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1200746244
MTHFR
0.807 0.080 1 11801287 missense variant C/T snv 4.0E-06 7.0E-06 11
rs749437638
ARVCF ; COMT
0.752 0.240 22 19968597 missense variant C/T snv 2.4E-05 1.4E-05 14
rs776943620
ACE
0.851 0.120 17 63477287 missense variant G/A snv 2.1E-05 7
rs6314
HTR2A
0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02 23
rs6198
NR3C1
0.724 0.480 5 143278056 3 prime UTR variant T/C snv 0.12 16
rs2230912
P2RX7 ; LOC105370032
0.752 0.280 12 121184393 missense variant A/G snv 0.13 0.12 16
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs1800497
ANKK1
0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs4570625
TPH2
0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31 23
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs6313
HTR2A
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82