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: rs778052047
rs778052047
DDC ; FIGNL1
1 1.000 0.080 7 50528268 missense variant C/T snv 4.0E-06 0.010 1.000 1 2015 2015
dbSNP: rs780737633
rs780737633
F2R
1 1.000 0.080 5 76733086 synonymous variant G/A;C snv 4.0E-06; 4.0E-06 0.010 1.000 1 2011 2011
dbSNP: rs7963720
rs7963720
TPH2
1 1.000 0.080 12 71972406 intron variant C/G;T snv 0.010 1.000 1 2008 2008
dbSNP: rs900418273
rs900418273
ANKK1
8 0.807 0.120 11 113393764 missense variant A/G snv 0.010 1.000 1 2015 2015
dbSNP: rs988712
rs988712
BDNF-AS
2 0.925 0.160 11 27541835 intron variant G/A;T snv 0.010 1.000 1 2016 2016
dbSNP: rs780726314
rs780726314
OPRM1
1 1.000 0.080 6 154039624 missense variant G/T snv 1.2E-05 7.0E-06 0.010 1.000 1 2002 2002
dbSNP: rs147247472
rs147247472
AGBL4 ; AGBL4-IT1
5 0.925 0.080 1 49441901 intron variant G/A snv 7.3E-04 0.700 1.000 1 2019 2019
dbSNP: rs62638690
rs62638690
OPRM1
2 0.925 0.080 6 154090110 missense variant G/T snv 5.6E-03 5.6E-03 0.010 1.000 1 2013 2013
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: 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: rs13306221
rs13306221
BDNF
4 0.851 0.120 11 27701142 intron variant C/T snv 5.9E-02 0.010 1.000 1 2011 2011
dbSNP: rs11606194
rs11606194
HTR3B
1 1.000 0.080 11 113910259 intron variant T/C snv 6.1E-02 0.010 1.000 1 2015 2015
dbSNP: rs2133896
rs2133896
ANKS1B
5 0.925 0.080 12 99455122 intron variant G/T snv 7.6E-02 0.700 1.000 1 2019 2019
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: rs10494334
rs10494334 		1 1.000 0.080 1 163535374 intergenic variant G/A snv 0.10 0.010 1.000 1 2010 2010
dbSNP: rs9479757
rs9479757
OPRM1
1 1.000 0.080 6 154090209 intron variant G/A snv 8.5E-02 0.10 0.010 1.000 1 2014 2014
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: rs2869577
rs2869577
RGS9
1 1.000 0.080 17 65199474 intron variant C/G snv 0.12 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: rs3823010
rs3823010
OPRM1
1 1.000 0.080 6 154058017 intron variant G/A snv 0.14 0.010 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 0.040 1.000 4 2011 2016
dbSNP: rs5326
rs5326
DRD1
6 0.851 0.160 5 175443193 5 prime UTR variant C/T snv 0.15 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: rs2283265
rs2283265
DRD2
12 0.776 0.160 11 113414814 intron variant C/A snv 0.16 0.010 1.000 1 2019 2019
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