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: 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: rs2234918
rs2234918
OPRD1
5 0.827 0.200 1 28863085 synonymous variant C/T snv 0.59 0.50 0.020 1.000 2 2002 2019
dbSNP: rs1042114
rs1042114
OPRD1
6 0.807 0.120 1 28812463 missense variant G/C;T snv 0.91 0.010 1.000 1 2002 2002
dbSNP: rs768020372
rs768020372
ALDH2
1 1.000 0.080 12 111792761 missense variant C/G;T snv 6.3E-06 0.010 1.000 1 2002 2002
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: rs1714984
rs1714984
MYOCD
1 1.000 0.080 17 12714384 intron variant A/G;T snv 0.010 1.000 1 2008 2008
dbSNP: rs1799913
rs1799913
TPH1
5 0.851 0.080 11 18025708 splice region variant G/A;T snv 0.39 0.33 0.010 1.000 1 2008 2008
dbSNP: rs1867898
rs1867898 		1 1.000 0.080 2 133762000 intergenic variant G/A snv 0.22 0.010 1.000 1 2008 2008
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: rs2236861
rs2236861
OPRD1
3 0.882 0.080 1 28813244 intron variant G/A snv 0.19 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: rs510769
rs510769
OPRM1
2 1.000 0.080 6 154040884 intron variant C/T snv 0.25 0.010 1.000 1 2008 2008
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: rs965972
rs965972 		1 1.000 0.080 1 193494720 intron variant G/A snv 0.86 0.010 1.000 1 2008 2008
dbSNP: rs1800497
rs1800497
ANKK1
56 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 0.040 1.000 4 2009 2019
dbSNP: rs6311
rs6311
HTR2A
41 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.020 1.000 2 2009 2014
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 2010 2010
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: rs11503014
rs11503014
GABRA2
2 1.000 0.080 4 46388848 5 prime UTR variant C/G snv 0.27 0.010 1.000 1 2010 2010
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 2010 2010
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: 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: rs1022563
rs1022563
PDYN-AS1
2 0.925 0.080 20 1973693 intron variant C/G;T snv 0.010 1.000 1 2011 2011
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: 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