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: rs2793094
rs2793094
DISC1 ; TSNAX-DISC1
3 0.925 0.080 1 231741236 intron variant G/A snv 0.97 0.010 1.000 1 2011 2011
dbSNP: rs5522
rs5522
NR3C2
19 0.732 0.320 4 148436323 missense variant C/T snv 0.88 0.89 0.050 1.000 5 2010 2015
dbSNP: rs174697
rs174697
ARVCF ; COMT
5 0.851 0.080 22 19966309 intron variant A/G snv 0.88 0.010 1.000 1 2012 2012
dbSNP: rs7103411
rs7103411
BDNF ; BDNF-AS
15 0.752 0.160 11 27678578 intron variant C/T snv 0.82 0.030 1.000 3 2010 2015
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: 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 0.010 1.000 1 2016 2016
dbSNP: rs2910164
rs2910164
MIR146A ; MIR3142HG
193 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 0.010 1.000 1 2018 2018
dbSNP: rs2070744
rs2070744
NOS3
54 0.608 0.680 7 150992991 intron variant C/T snv 0.70 0.010 1.000 1 2011 2011
dbSNP: rs7997012
rs7997012
HTR2A
11 0.807 0.080 13 46837850 intron variant A/G snv 0.69 0.010 1.000 1 2013 2013
dbSNP: rs4580704
rs4580704
CLOCK
13 0.790 0.200 4 55460540 intron variant G/C snv 0.69 0.010 1.000 1 2019 2019
dbSNP: rs3096140
rs3096140
GDNF ; GDNF-AS1
5 0.882 0.080 5 37832731 intron variant G/A snv 0.69 0.010 < 0.001 1 2013 2013
dbSNP: rs386231
rs386231
NOS1AP
4 0.882 0.080 1 162356033 intron variant C/T snv 0.68 0.010 1.000 1 2013 2013
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 2018 2018
dbSNP: rs10410544
rs10410544
SIRT2
6 0.827 0.120 19 38894892 intron variant T/C snv 0.68 0.67 0.010 1.000 1 2013 2013
dbSNP: rs948854
rs948854
GAL ; LOC107984343
4 0.882 0.200 11 68682735 upstream gene variant C/T snv 0.65 0.010 1.000 1 2018 2018
dbSNP: rs9296158
rs9296158
FKBP5 ; LOC112267956
16 0.763 0.080 6 35599305 intron variant A/G snv 0.65 0.010 1.000 1 2012 2012
dbSNP: rs156243
rs156243 		6 0.925 0.080 6 104416939 intergenic variant G/A snv 0.65 0.010 1.000 1 2014 2014
dbSNP: rs3916966
rs3916966 		4 0.882 0.080 13 105458546 upstream gene variant C/A snv 0.63 0.010 < 0.001 1 2010 2010
dbSNP: rs242941
rs242941
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
9 0.790 0.200 17 45815154 intron variant A/C snv 0.62 0.020 1.000 2 2013 2015
dbSNP: rs11824092
rs11824092
ARNTL
7 0.925 0.080 11 13324747 intron variant T/C snv 0.62 0.010 1.000 1 2014 2014
dbSNP: rs10434
rs10434
VEGFA
17 0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59 0.010 1.000 1 2014 2014
dbSNP: rs16944
rs16944
IL1B
92 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.020 1.000 2 2016 2019
dbSNP: rs4305745
rs4305745 		4 0.882 0.080 6 132572573 downstream gene variant G/A snv 0.55 0.010 1.000 1 2010 2010
dbSNP: rs1415259
rs1415259
NOS1AP ; LOC105371475
5 0.925 0.080 1 162115519 intron variant C/T snv 0.54 0.010 1.000 1 2015 2015