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: rs2736100
rs2736100
TERT
83 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 0.010 1.000 1 2019 2019
dbSNP: rs324420
rs324420
FAAH
48 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 0.010 1.000 1 2016 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: rs10852889
rs10852889
ALOX12 ; ALOX12-AS1
1 1.000 0.040 17 6997526 intron variant C/A;G;T snv 0.010 1.000 1 2015 2015
dbSNP: rs2251177
rs2251177
DRD3
1 1.000 0.040 3 114139503 missense variant C/A;T snv 8.0E-06; 0.99 0.010 1.000 1 2014 2014
dbSNP: rs27072
rs27072
SLC6A3
11 0.807 0.120 5 1394407 3 prime UTR variant C/A;T snv 0.010 1.000 1 2013 2013
dbSNP: rs2794520
rs2794520 		9 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 0.010 1.000 1 2018 2018
dbSNP: rs3100127
rs3100127 		1 1.000 0.040 1 202191842 upstream gene variant C/A;T snv 0.700 1.000 1 2015 2015
dbSNP: rs6189
rs6189
NR3C1
6 0.827 0.240 5 143400774 missense variant C/A;T snv 4.0E-06; 1.8E-02 0.010 1.000 1 2018 2018
dbSNP: rs6812849
rs6812849
TLL1
1 1.000 0.040 4 165951384 intron variant C/A;T snv 0.800 1.000 1 2013 2013
dbSNP: rs717947
rs717947 		1 1.000 0.040 4 33652135 intron variant C/A;T snv 0.010 1.000 1 2015 2015
dbSNP: rs2267735
rs2267735
ADCYAP1R1
2 0.925 0.120 7 31095890 intron variant C/G snv 0.47 0.050 0.800 5 2013 2017
dbSNP: rs6295
rs6295
HTR1A
40 0.645 0.200 5 63962738 intron variant C/G snv 0.49 0.020 1.000 2 2016 2019
dbSNP: rs1800795
rs1800795
IL6 ; STEAP1B ; IL6-AS1
140 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 < 0.001 1 2019 2019
dbSNP: rs1143633
rs1143633
IL1B
11 0.752 0.280 2 112832890 intron variant C/G;T snv 0.010 1.000 1 2017 2017
dbSNP: rs1876831
rs1876831
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
4 0.925 0.040 17 45830379 non coding transcript exon variant C/G;T snv 4.4E-06; 0.14 0.010 1.000 1 2014 2014
dbSNP: rs4606
rs4606
RGS2
16 0.752 0.120 1 192812042 3 prime UTR variant C/G;T snv 0.010 1.000 1 2009 2009
dbSNP: rs7866350
rs7866350
TBC1D2
1 1.000 0.040 9 98221544 intron variant C/G;T snv 0.20 0.700 1.000 1 2015 2015
dbSNP: rs6265
rs6265
BDNF ; BDNF-AS
272 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.100 0.850 20 2006 2019
dbSNP: rs759834365
rs759834365
BDNF ; BDNF-AS
237 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 0.100 0.824 17 2006 2019
dbSNP: rs1033962
rs1033962
PRTFDC1
1 1.000 0.040 10 24927877 intron variant C/T snv 0.33 0.700 1.000 1 2015 2015
dbSNP: rs1049353
rs1049353
CNR1
42 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 0.010 1.000 1 2019 2019
dbSNP: rs1205
rs1205
CRP
46 0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 0.010 1.000 1 2018 2018
dbSNP: rs1374141592
rs1374141592
FLT4
1 1.000 0.040 5 180630561 missense variant C/T snv 7.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs17070145
rs17070145
WWC1
10 0.790 0.120 5 168418786 intron variant C/T snv 0.43 0.010 1.000 1 2018 2018