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: rs1801028
rs1801028
DRD2
24 0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02 0.010 1.000 1 1998 1998
dbSNP: rs1799971
rs1799971
OPRM1
95 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 0.010 1.000 1 2004 2004
dbSNP: rs104894685
rs104894685
FTL
4 0.925 0.120 19 48966317 missense variant G/A snv 4.0E-06 1.4E-05 0.010 1.000 1 2005 2005
dbSNP: rs1695
rs1695
GSTP1
188 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2005 2005
dbSNP: rs1217691063
rs1217691063
MTHFR
614 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.010 1.000 1 2006 2006
dbSNP: rs2076369
rs2076369
PICK1
3 0.925 0.040 22 38067645 non coding transcript exon variant T/A;G snv 0.010 1.000 1 2007 2007
dbSNP: rs3745274
rs3745274
CYP2B6
30 0.672 0.480 19 41006936 missense variant G/A;T snv 4.0E-06; 0.27 0.010 1.000 1 2007 2007
dbSNP: rs713729
rs713729
PICK1
2 1.000 0.040 22 38059462 intron variant T/A snv 0.20 0.010 1.000 1 2007 2007
dbSNP: rs737864
rs737864
COMT ; TXNRD2
2 1.000 0.040 22 19942636 intron variant C/T snv 0.23 0.010 1.000 1 2007 2007
dbSNP: rs737865
rs737865
COMT ; TXNRD2
11 0.763 0.240 22 19942598 intron variant A/G snv 0.23 0.010 1.000 1 2007 2007
dbSNP: rs951436
rs951436 		3 0.925 0.040 1 163063552 regulatory region variant A/C snv 0.42 0.010 1.000 1 2007 2007
dbSNP: rs6280
rs6280
DRD3
57 0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 0.030 1.000 3 2004 2008
dbSNP: rs135745
rs135745 		13 0.763 0.200 22 38287631 downstream gene variant G/C snv 0.48 0.010 < 0.001 1 2008 2008
dbSNP: rs2619538
rs2619538
DTNBP1
4 0.882 0.040 6 15664978 upstream gene variant A/T snv 0.54 0.010 1.000 1 2008 2008
dbSNP: rs2619539
rs2619539
DTNBP1
3 0.925 0.040 6 15620624 intron variant C/A;G snv 0.010 1.000 1 2008 2008
dbSNP: rs3213207
rs3213207
DTNBP1
11 0.776 0.120 6 15627871 intron variant T/C snv 8.7E-02 0.010 1.000 1 2008 2008
dbSNP: rs6994992
rs6994992
NRG1
13 0.790 0.120 8 31638065 upstream gene variant C/A;T snv 0.020 1.000 2 2008 2009
dbSNP: rs1421292
rs1421292 		3 0.925 0.040 13 105545886 intergenic variant T/A snv 0.39 0.010 1.000 1 2009 2009
dbSNP: rs16147
rs16147
NPY ; LOC107986777
18 0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48 0.010 1.000 1 2009 2009
dbSNP: rs2391191
rs2391191
DAOA ; DAOA-AS1
7 0.807 0.080 13 105467097 missense variant G/A snv 0.40 0.32 0.010 1.000 1 2009 2009
dbSNP: rs3800373
rs3800373
FKBP5 ; LOC101929309
22 0.752 0.200 6 35574699 3 prime UTR variant C/A snv 0.68 0.010 1.000 1 2009 2009
dbSNP: rs3916965
rs3916965 		4 0.882 0.040 13 105451011 intergenic variant C/T snv 0.31 0.010 1.000 1 2009 2009
dbSNP: rs7687423
rs7687423
NPY1R
3 0.925 0.080 4 163329645 intron variant A/G snv 0.53 0.010 1.000 1 2009 2009
dbSNP: rs778293
rs778293 		7 0.807 0.120 13 105516850 intergenic variant C/A;T snv 0.010 1.000 1 2009 2009
dbSNP: rs947267
rs947267
DAOA ; DAOA-AS1
4 0.882 0.040 13 105487313 intron variant T/G snv 0.51 0.010 1.000 1 2009 2009