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: rs10828317
rs10828317
PIP4K2A
9 0.776 0.280 10 22550699 missense variant T/C snv 0.010 < 0.001 1 2014 2014
dbSNP: rs2230469
rs2230469
PIP4K2A
3 0.882 0.160 10 22550699 missense variant T/C snv 0.27 0.24 0.010 < 0.001 1 2014 2014
dbSNP: rs334558
rs334558
GSK3B ; LOC107986119
20 0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51 0.010 < 0.001 1 2019 2019
dbSNP: rs3730358
rs3730358
AKT1
14 0.724 0.360 14 104780070 intron variant G/A;C snv 0.16; 4.0E-03 0.010 < 0.001 1 2019 2019
dbSNP: rs5443
rs5443
GNB3 ; CDCA3
106 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 0.010 < 0.001 1 2007 2007
dbSNP: rs6275
rs6275
DRD2
7 0.851 0.160 11 113412755 synonymous variant A/G snv 0.64 0.58 0.010 < 0.001 1 2007 2007
dbSNP: rs7620754
rs7620754
LOC107986115
2 0.925 0.120 3 114229128 intron variant T/C snv 0.24 0.010 < 0.001 1 2009 2009
dbSNP: rs76980269
rs76980269
NOS1
10 0.763 0.280 12 117330794 synonymous variant G/A snv 2.8E-05 4.2E-05 0.010 < 0.001 1 2004 2004
dbSNP: rs905568
rs905568
LOC107986115
2 0.925 0.120 3 114232449 non coding transcript exon variant C/A;G;T snv 0.010 < 0.001 1 2009 2009
dbSNP: rs4880
rs4880
SOD2
131 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 0.020 0.500 2 2008 2010
dbSNP: rs6314
rs6314
HTR2A
23 0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02 0.020 0.500 2 2001 2005
dbSNP: rs995922697
rs995922697
GPX1
15 0.724 0.560 3 49357413 missense variant A/G snv 4.1E-06 0.020 0.500 2 2006 2010
dbSNP: rs4680
rs4680
COMT ; MIR4761
249 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 0.050 0.600 5 2005 2016
dbSNP: rs953038635
rs953038635
SOD2
51 0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 0.090 0.778 9 2000 2015
dbSNP: rs6280
rs6280
DRD3
57 0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 0.100 0.800 15 1997 2012
dbSNP: rs6265
rs6265
BDNF ; BDNF-AS
272 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.050 0.800 5 2004 2014
dbSNP: rs759834365
rs759834365
BDNF ; BDNF-AS
237 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 0.050 0.800 5 2004 2014
dbSNP: rs1258159645
rs1258159645
NQO1
37 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 0.030 1.000 3 2006 2010
dbSNP: rs1800566
rs1800566
NQO1
59 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 0.030 1.000 3 2006 2010
dbSNP: rs1801028
rs1801028
DRD2
24 0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02 0.030 1.000 3 2001 2005
dbSNP: rs2445142
rs2445142
HSPG2
2 0.925 0.120 1 21899250 intron variant G/A;C snv 0.030 1.000 3 2010 2018
dbSNP: rs1182593032
rs1182593032
NQO1
4 0.851 0.200 16 69718516 missense variant A/G snv 0.020 1.000 2 2008 2010
dbSNP: rs6277
rs6277
DRD2
36 0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 0.020 1.000 2 2007 2013
dbSNP: rs6313
rs6313
HTR2A
82 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 0.020 1.000 2 2005 2009
dbSNP: rs767413934
rs767413934
DRD2
2 0.925 0.120 11 113424539 missense variant G/A snv 4.0E-06 0.020 1.000 2 2008 2008