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: rs6277
rs6277
DRD2
36 0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 0.040 1.000 4 2008 2012
dbSNP: rs1217691063
rs1217691063
MTHFR
614 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.030 1.000 3 2006 2018
dbSNP: rs201745983
rs201745983
ALDH2
14 0.752 0.200 12 111783219 missense variant G/A snv 6.8E-05 7.7E-05 0.030 1.000 3 2010 2018
dbSNP: rs9939609
rs9939609
FTO
98 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.030 1.000 3 2011 2014
dbSNP: rs1000579
rs1000579
STX18-AS1
3 1.000 0.080 4 4717767 intron variant A/G snv 0.44 0.800 1.000 2 2012 2017
dbSNP: rs1042363
rs1042363
AKAP12
4 0.882 0.080 6 151356693 3 prime UTR variant T/C snv 0.020 1.000 2 2005 2006
dbSNP: rs1042364
rs1042364
ADH4 ; LOC100507053
1 1.000 0.080 4 99124423 stop gained T/A;C snv 0.78 0.020 1.000 2 2011 2016
dbSNP: rs1076560
rs1076560
DRD2
11 0.776 0.120 11 113412966 intron variant C/A snv 0.16 0.020 1.000 2 2007 2014
dbSNP: rs1079597
rs1079597
DRD2
5 0.827 0.080 11 113425564 intron variant C/T snv 0.18 0.020 1.000 2 2014 2017
dbSNP: rs1176744
rs1176744
HTR3B
19 0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 0.020 1.000 2 2011 2013
dbSNP: rs1614972
rs1614972
ADH1B ; ADH1C
4 0.925 0.160 4 99336998 intron variant C/T snv 0.38 0.710 1.000 2 2013 2014
dbSNP: rs1800759
rs1800759
ADH4 ; LOC100507053
4 0.925 0.120 4 99144358 intron variant T/G snv 0.49 0.020 1.000 2 2006 2011
dbSNP: rs1997794
rs1997794
PDYN ; PDYN-AS1
4 0.851 0.120 20 1994212 5 prime UTR variant T/C snv 0.50 0.020 1.000 2 2013 2018
dbSNP: rs2173201
rs2173201
ADH1B
3 1.000 0.080 4 99329813 intron variant C/A snv 0.30 0.710 1.000 2 2014 2014
dbSNP: rs2235751
rs2235751
PDYN ; PDYN-AS1
3 0.882 0.120 20 1989288 intron variant A/G snv 0.40 0.020 1.000 2 2013 2017
dbSNP: rs2281285
rs2281285
PDYN ; PDYN-AS1
2 0.925 0.080 20 1991814 intron variant T/C snv 0.16 0.020 1.000 2 2013 2015
dbSNP: rs248793
rs248793
SRD5A1 ; NSUN2
1 1.000 0.080 5 6633666 synonymous variant C/G snv 0.55 0.58 0.020 1.000 2 2011 2014
dbSNP: rs29220
rs29220
GABBR1
1 1.000 0.080 6 29621889 intron variant C/G snv 0.31 0.020 1.000 2 2016 2018
dbSNP: rs3027172
rs3027172
PER1
2 0.925 0.080 17 8152405 missense variant A/G snv 0.38 0.17 0.020 1.000 2 2011 2015
dbSNP: rs324650
rs324650
CHRM2 ; LOC349160
5 0.827 0.080 7 137008914 intron variant T/A snv 0.55 0.020 1.000 2 2004 2011
dbSNP: rs35385902
rs35385902
ADH1B ; ADH1C
9 0.807 0.240 4 99347122 missense variant C/A;T snv 2.0E-05; 1.1E-03 0.020 1.000 2 2005 2018
dbSNP: rs363387
rs363387
SLC18A2 ; LOC105378500
1 1.000 0.080 10 117244053 synonymous variant T/A;C;G snv 4.0E-06; 7.9E-02 0.020 1.000 2 2005 2013
dbSNP: rs3762894
rs3762894
ADH4 ; LOC100507053
2 1.000 0.080 4 99144933 intron variant T/C snv 0.19 0.020 1.000 2 2011 2011
dbSNP: rs6280
rs6280
DRD3
57 0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 0.020 1.000 2 2006 2014
dbSNP: rs6350
rs6350
SLC6A3
3 0.882 0.080 5 1443084 missense variant G/A;C snv 5.6E-02; 6.8E-05 0.020 1.000 2 2009 2017