Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs5522
rs5522
NR3C2
19 0.732 0.320 4 148436323 missense variant C/T snv 0.88 0.89 0.010 1.000 1 2010 2010
dbSNP: rs7973260
rs7973260
KSR2
7 0.851 0.120 12 117937681 intron variant A/G snv 0.83 0.010 1.000 1 2017 2017
dbSNP: rs7103411
rs7103411
BDNF ; BDNF-AS
15 0.752 0.160 11 27678578 intron variant C/T snv 0.82 0.010 1.000 1 2012 2012
dbSNP: rs2794521
rs2794521
CRP
15 0.742 0.480 1 159715306 upstream gene variant C/T snv 0.78 0.010 1.000 1 2019 2019
dbSNP: rs161645
rs161645
LOC105379109
2 1.000 0.040 5 104734216 intron variant A/G snv 0.77 0.010 1.000 1 2013 2013
dbSNP: rs738499
rs738499
TEF ; LOC105373042
9 0.851 0.120 22 41381096 intron variant G/T snv 0.76 0.010 1.000 1 2012 2012
dbSNP: rs1800795
rs1800795
IL6 ; STEAP1B ; IL6-AS1
140 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.030 1.000 3 2010 2016
dbSNP: rs3800373
rs3800373
FKBP5 ; LOC101929309
22 0.752 0.200 6 35574699 3 prime UTR variant C/A snv 0.68 0.010 1.000 1 2019 2019
dbSNP: rs948854
rs948854
GAL ; LOC107984343
4 0.882 0.200 11 68682735 upstream gene variant C/T snv 0.65 0.020 1.000 2 2010 2018
dbSNP: rs9296158
rs9296158
FKBP5 ; LOC112267956
16 0.763 0.080 6 35599305 intron variant A/G snv 0.65 0.020 1.000 2 2015 2019
dbSNP: rs1008805
rs1008805
CYP19A1 ; MIR4713HG
7 0.851 0.160 15 51257402 intron variant G/A snv 0.64 0.010 1.000 1 2016 2016
dbSNP: rs680244
rs680244
CHRNA5
4 0.882 0.120 15 78578946 intron variant T/C snv 0.60 0.010 1.000 1 2015 2015
dbSNP: rs1946518
rs1946518
IL18
46 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.010 1.000 1 2017 2017
dbSNP: rs699
rs699
AGT
134 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2008 2008
dbSNP: rs16944
rs16944
IL1B
92 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.030 1.000 3 2015 2019
dbSNP: rs3756290
rs3756290
RAPGEF6
1 5 131616057 intron variant A/G snv 0.56 0.010 < 0.001 1 2017 2017
dbSNP: rs5440
rs5440
GNB3 ; P3H3
1 12 6839735 3 prime UTR variant A/G snv 0.56 0.010 1.000 1 2014 2014
dbSNP: rs165599
rs165599
ARVCF ; COMT
27 0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 0.010 1.000 1 2010 2010
dbSNP: rs4290270
rs4290270
TPH2
17 0.724 0.320 12 72022455 synonymous variant A/T snv 0.57 0.55 0.010 < 0.001 1 2018 2018
dbSNP: rs4481363
rs4481363
LOC105377703
1 5 165047713 intron variant C/A snv 0.55 0.010 < 0.001 1 2017 2017
dbSNP: rs2227631
rs2227631
SERPINE1
13 0.742 0.200 7 101126257 upstream gene variant A/G snv 0.54 0.010 1.000 1 2012 2012
dbSNP: rs33388
rs33388
NR3C1
12 0.776 0.360 5 143317730 intron variant A/T snv 0.53 0.010 1.000 1 2011 2011
dbSNP: rs10914456
rs10914456
HCRTR1
2 1.000 0.040 1 31622570 intron variant T/C snv 0.51 0.010 1.000 1 2019 2019
dbSNP: rs10055255
rs10055255
CRHBP
2 1.000 0.040 5 76968168 intron variant A/T snv 0.50 0.010 1.000 1 2014 2014
dbSNP: rs6295
rs6295
HTR1A
40 0.645 0.200 5 63962738 intron variant C/G snv 0.49 0.030 1.000 3 2013 2015