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: rs1040288
rs1040288
NR3C2
3 1.000 0.040 4 148126966 intron variant G/C snv 0.49 0.010 1.000 1 2014 2014
dbSNP: rs11030096
rs11030096
BDNF-AS
3 0.925 0.160 11 27643996 intron variant T/A;C snv 0.010 1.000 1 2016 2016
dbSNP: rs12043259
rs12043259
NFASC
2 1 204858913 intron variant C/G snv 0.11 0.700 1.000 1 2013 2013
dbSNP: rs1333048
rs1333048
CDKN2B-AS1
24 0.683 0.320 9 22125348 intron variant A/C snv 0.44 0.010 1.000 1 2020 2020
dbSNP: rs1409568
rs1409568 		2 1.000 0.040 10 118871273 intron variant T/C snv 8.2E-02 0.010 1.000 1 2018 2018
dbSNP: rs17664708
rs17664708
NRG1
2 1.000 0.080 8 32579499 intron variant C/T snv 1.0E-01 0.010 1.000 1 2012 2012
dbSNP: rs2023239
rs2023239
CNR1
20 0.724 0.160 6 88150763 intron variant T/C snv 0.21 0.010 1.000 1 2012 2012
dbSNP: rs2070762
rs2070762
TH
5 0.925 0.080 11 2165105 intron variant A/G snv 0.43 0.010 1.000 1 2018 2018
dbSNP: rs2073837
rs2073837
DBH ; DBH-AS1
1 9 133657806 intron variant G/A snv 0.31 0.010 1.000 1 2018 2018
dbSNP: rs2251214
rs2251214
SYT1
7 0.827 0.040 12 79430071 intron variant A/G;T snv 0.010 1.000 1 2019 2019
dbSNP: rs2283265
rs2283265
DRD2
12 0.776 0.160 11 113414814 intron variant C/A snv 0.16 0.010 1.000 1 2015 2015
dbSNP: rs230530
rs230530
NFKB1
4 0.882 0.080 4 102532823 intron variant A/G snv 0.37 0.010 1.000 1 2015 2015
dbSNP: rs2377339
rs2377339
NCK2
2 2 105840835 intron variant A/G snv 4.8E-02 0.700 1.000 1 2013 2013
dbSNP: rs4436578
rs4436578
DRD2
4 0.925 0.080 11 113436043 intron variant C/T snv 0.73 0.010 1.000 1 2020 2020
dbSNP: rs4648318
rs4648318
DRD2
2 1.000 0.080 11 113442667 intron variant T/C snv 0.33 0.010 1.000 1 2020 2020
dbSNP: rs604300
rs604300
MGLL
3 1.000 0.080 3 127724009 intron variant A/G snv 0.91 0.010 1.000 1 2015 2015
dbSNP: rs678849
rs678849
OPRD1
5 0.882 0.120 1 28818676 intron variant C/T snv 0.44 0.010 1.000 1 2016 2016
dbSNP: rs9444584
rs9444584
CNR1
4 0.882 0.160 6 88152840 intron variant C/T snv 0.30 0.010 1.000 1 2012 2012
dbSNP: rs9450898
rs9450898
CNR1
3 0.925 0.160 6 88154344 intron variant C/T snv 0.21 0.010 1.000 1 2012 2012
dbSNP: rs382140
rs382140 		1 7 108141755 intergenic variant A/G snv 0.74 0.010 1.000 1 2012 2012
dbSNP: rs1799971
rs1799971
OPRM1
95 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 0.090 1.000 9 2004 2019
dbSNP: rs324420
rs324420
FAAH
48 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 0.050 1.000 5 2004 2020
dbSNP: rs4680
rs4680
COMT ; MIR4761
249 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 0.040 1.000 4 2004 2013
dbSNP: rs1800497
rs1800497
ANKK1
56 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 0.020 1.000 2 2013 2017
dbSNP: rs1044396
rs1044396
CHRNA4
17 0.742 0.240 20 63349782 missense variant G/A;C snv 0.47; 6.1E-05 0.010 1.000 1 2012 2012