Disease: Depressive Symptoms
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10914456
HCRTR1
1.000 0.040 1 31622570 intron variant T/C snv 0.51 2
rs6994992
NRG1
0.790 0.120 8 31638065 upstream gene variant C/A;T snv 13
rs3800373
LOC101929309 ; FKBP5
0.752 0.200 6 35574699 3 prime UTR variant C/A snv 0.68 22
rs9296158
FKBP5 ; LOC112267956
0.763 0.080 6 35599305 intron variant A/G snv 0.65 16
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs738499
TEF ; LOC105373042
0.851 0.120 22 41381096 intron variant G/T snv 0.76 9
rs110402
CRHR1 ; LINC02210-CRHR1 ; MAPT-AS1
0.790 0.120 17 45802681 intron variant G/A;C snv 12
rs6314
HTR2A
0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02 23
rs6313
HTR2A
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs6311
HTR2A
0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs2535629
ITIH3
0.827 0.040 3 52799203 intron variant G/A;C snv 9
rs776943620
ACE
0.851 0.120 17 63477287 missense variant G/A snv 2.1E-05 7
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs5443
CDCA3 ; GNB3
0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs4570625
TPH2
0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs4290270
TPH2
0.724 0.320 12 72022455 synonymous variant A/T snv 0.57 0.55 17
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157