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: rs1800497
rs1800497
ANKK1
56 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 0.080 0.875 8 2009 2019
dbSNP: rs4680
rs4680
COMT ; MIR4761
249 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 0.020 1.000 2 2011 2013
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 2009 2019
dbSNP: rs900418273
rs900418273
ANKK1
8 0.807 0.120 11 113393764 missense variant A/G snv 0.020 1.000 2 2011 2013
dbSNP: rs147347002
rs147347002
DRD2
1 1.000 11 113416879 synonymous variant G/A snv 1.9E-04 6.6E-04 0.010 1.000 1 2007 2007
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 2014 2014
dbSNP: rs1805055
rs1805055
HTR2A
3 0.882 0.120 13 46895833 missense variant G/C;T snv 2.0E-05; 1.8E-02 0.010 1.000 1 2007 2007
dbSNP: rs6265
rs6265
BDNF ; BDNF-AS
272 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.010 1.000 1 2012 2012
dbSNP: rs6305
rs6305
HTR2A
3 0.882 0.040 13 46892487 synonymous variant G/A snv 1.8E-02 1.7E-02 0.010 1.000 1 2007 2007
dbSNP: rs6313
rs6313
HTR2A
82 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 0.010 1.000 1 2007 2007
dbSNP: rs6314
rs6314
HTR2A
23 0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02 0.010 1.000 1 2007 2007
dbSNP: rs759834365
rs759834365
BDNF ; BDNF-AS
237 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 0.010 1.000 1 2012 2012
dbSNP: rs762199332
rs762199332
SLC6A3
1 1.000 5 1432601 synonymous variant G/A snv 4.0E-06 0.010 1.000 1 2007 2007
dbSNP: rs893924483
rs893924483
BDNF ; BDNF-AS
23 0.716 0.280 11 27658285 missense variant C/A;T snv 4.0E-06 1.4E-05 0.010 1.000 1 2011 2011