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: rs1176744
rs1176744
HTR3B
19 0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 0.010 1.000 1 2011 2011
dbSNP: rs4790953
rs4790953 		4 0.851 0.160 17 65230912 downstream gene variant A/C snv 0.17 0.010 1.000 1 2015 2015
dbSNP: rs884344
rs884344
GDNF ; GDNF-AS1
5 0.882 0.120 5 37824138 intron variant A/C snv 0.33 0.010 1.000 1 2013 2013
dbSNP: rs1122079
rs1122079
RGS9
1 1.000 0.080 17 65218385 intron variant A/C;T snv 0.010 1.000 1 2015 2015
dbSNP: rs1344706
rs1344706
ZNF804A
21 0.701 0.160 2 184913701 intron variant A/C;T snv 0.010 1.000 1 2015 2015
dbSNP: rs1799971
rs1799971
OPRM1
95 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 0.070 0.857 7 2001 2017
dbSNP: rs10078866
rs10078866
DRD1
2 1.000 0.080 5 175445317 upstream gene variant A/G snv 5.2E-02 0.010 1.000 1 2015 2015
dbSNP: rs11030104
rs11030104
BDNF ; BDNF-AS
12 0.790 0.240 11 27662970 intron variant A/G snv 0.16 0.010 1.000 1 2016 2016
dbSNP: rs12364283
rs12364283
DRD2 ; LOC105369501
3 0.925 0.080 11 113476233 upstream gene variant A/G snv 5.8E-02 0.010 1.000 1 2019 2019
dbSNP: rs187269
rs187269
GABRB2
6 0.827 0.160 5 161329618 3 prime UTR variant A/G snv 0.34 0.010 1.000 1 2015 2015
dbSNP: rs2292592
rs2292592
RGS9
1 1.000 0.080 17 65208091 intron variant A/G snv 0.12 0.010 1.000 1 2015 2015
dbSNP: rs4906902
rs4906902
GABRB3
14 0.724 0.200 15 26774621 intron variant A/G snv 0.15 0.010 1.000 1 2014 2014
dbSNP: rs581111
rs581111
OPRD1
1 1.000 0.080 1 28848861 intron variant A/G snv 0.63 0.010 1.000 1 2014 2014
dbSNP: rs8070231
rs8070231
RGS9
1 1.000 0.080 17 65198827 intron variant A/G snv 0.20 0.010 1.000 1 2015 2015
dbSNP: rs900418273
rs900418273
ANKK1
8 0.807 0.120 11 113393764 missense variant A/G snv 0.010 1.000 1 2015 2015
dbSNP: rs910080
rs910080
PDYN ; PDYN-AS1
4 0.851 0.120 20 1979580 3 prime UTR variant A/G snv 0.35 0.010 1.000 1 2011 2011
dbSNP: rs950302
rs950302
GPA33 ; DUSP27
1 1.000 0.080 1 167114567 intron variant A/G snv 0.47 0.010 1.000 1 2010 2010
dbSNP: rs9825563
rs9825563
DRD3
2 1.000 0.080 3 114181373 intron variant A/G snv 0.36 0.010 1.000 1 2014 2014
dbSNP: rs1389752
rs1389752
MPDZ
2 0.925 0.080 9 13235288 intron variant A/G;T snv 0.010 1.000 1 2015 2015
dbSNP: rs1714984
rs1714984
MYOCD
1 1.000 0.080 17 12714384 intron variant A/G;T snv 0.010 1.000 1 2008 2008
dbSNP: rs265981
rs265981
DRD1
3 0.925 0.080 5 175443899 5 prime UTR variant A/G;T snv 0.010 < 0.001 1 2015 2015
dbSNP: rs2910709
rs2910709
GDNF-AS1
4 0.882 0.120 5 37811762 non coding transcript exon variant A/G;T snv 0.010 1.000 1 2013 2013
dbSNP: rs1986513
rs1986513 		1 1.000 0.080 4 125146073 intergenic variant A/T snv 8.9E-02 0.010 1.000 1 2008 2008
dbSNP: rs4290270
rs4290270
TPH2
17 0.724 0.320 12 72022455 synonymous variant A/T snv 0.57 0.55 0.010 1.000 1 2008 2008
dbSNP: rs1076560
rs1076560
DRD2
11 0.776 0.120 11 113412966 intron variant C/A snv 0.16 0.010 1.000 1 2019 2019