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: 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: rs1360780
rs1360780
FKBP5 ; LOC112267956
31 0.708 0.320 6 35639794 intron variant T/A;C snv 0.060 1.000 6 2013 2019
dbSNP: rs9470080
rs9470080
FKBP5
13 0.827 0.080 6 35678658 intron variant T/A;C snv 0.060 0.833 6 2008 2019
dbSNP: rs53576
rs53576
CAV3 ; OXTR
42 0.641 0.320 3 8762685 intron variant A/G;T snv 0.030 1.000 3 2017 2020
dbSNP: rs2400707
rs2400707
ADRB2
3 1.000 0.040 5 148825489 5 prime UTR variant A/G;T snv 0.020 1.000 2 2014 2017
dbSNP: rs363276
rs363276
SLC18A2
1 1.000 0.040 10 117274298 intron variant T/C;G snv 0.020 1.000 2 2014 2018
dbSNP: rs7208505
rs7208505
SKA2
2 1.000 0.040 17 59110368 3 prime UTR variant G/A;C;T snv 0.020 0.500 2 2016 2016
dbSNP: rs1042357
rs1042357
ALOX12 ; ALOX12-AS1
2 0.925 0.040 17 7001742 synonymous variant T/C;G snv 0.59 0.010 1.000 1 2015 2015
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: rs110402
rs110402
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
12 0.790 0.120 17 45802681 intron variant G/A;C snv 0.010 1.000 1 2017 2017
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: rs182455
rs182455
STMN1 ; LOC105376885
2 0.925 0.120 1 25908492 upstream gene variant A/G;T snv 0.010 1.000 1 2013 2013
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: 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: rs2267715
rs2267715
CRHR2
1 1.000 0.040 7 30676471 intron variant G/A;C snv 0.010 1.000 1 2020 2020
dbSNP: rs2295633
rs2295633
FAAH
7 0.827 0.120 1 46408711 intron variant A/G;T snv 0.010 1.000 1 2012 2012
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: rs3091244
rs3091244
CRP
17 0.724 0.280 1 159714875 upstream gene variant G/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: rs3749034
rs3749034
GAD1
6 0.827 0.040 2 170816965 5 prime UTR variant G/A;T snv 0.010 1.000 1 2019 2019
dbSNP: rs406001
rs406001 		1 1.000 0.040 7 51938719 intergenic variant T/A;C snv 0.800 1.000 1 2013 2013
dbSNP: rs451275
rs451275
SPRY4-AS1
1 1.000 0.040 5 142392033 intron variant C/T snv 0.010 1.000 1 2013 2013
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: rs4775301
rs4775301
RORA
2 0.925 0.040 15 60834660 intron variant T/C;G snv 0.700 1.000 1 2013 2013