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: rs10009145
rs10009145
ADH4 ; LOC100507053
1 1.000 0.080 4 99126778 intron variant G/A snv 0.39 0.34 0.010 1.000 1 2012 2012
dbSNP: rs10051667
rs10051667
GABRB2
2 0.925 0.080 5 161471322 intron variant T/C snv 0.12 0.010 1.000 1 2015 2015
dbSNP: rs10160548
rs10160548
HTR3A
1 1.000 0.080 11 113985959 intron variant G/T snv 0.54 0.010 1.000 1 2013 2013
dbSNP: rs1017418
rs1017418
LOC730100
1 1.000 0.080 2 51821024 intron variant G/A;C snv 0.010 1.000 1 2007 2007
dbSNP: rs1034866440
rs1034866440
AR
4 0.851 0.160 X 67643401 missense variant G/A snv 5.7E-06 0.010 1.000 1 2012 2012
dbSNP: rs1034936
rs1034936
CACNA1C
3 0.882 0.080 12 2551994 intron variant C/T snv 0.61 0.010 1.000 1 2020 2020
dbSNP: rs1039002
rs1039002
PDE10A
5 0.851 0.080 6 165741969 intron variant G/A;T snv 0.010 1.000 1 2011 2011
dbSNP: rs1042114
rs1042114
OPRD1
6 0.807 0.120 1 28812463 missense variant G/C;T snv 0.91 0.010 1.000 1 2008 2008
dbSNP: rs1042173
rs1042173
SLC6A4
14 0.763 0.320 17 30197993 3 prime UTR variant A/C snv 0.40 0.010 1.000 1 2013 2013
dbSNP: rs10496768
rs10496768
THSD7B
1 1.000 0.080 2 137322384 intron variant G/A snv 9.5E-02 0.010 1.000 1 2011 2011
dbSNP: rs10514299
rs10514299
TMEM161B-AS1
6 0.827 0.120 5 88367793 intron variant C/T snv 0.21 0.010 1.000 1 2018 2018
dbSNP: rs1051740
rs1051740
EPHX1
56 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.010 1.000 1 2013 2013
dbSNP: rs10889635
rs10889635
SGIP1
1 1.000 0.080 1 66609892 intron variant G/A snv 0.65 0.010 1.000 1 2016 2016
dbSNP: rs10892169
rs10892169
DSCAML1
1 1.000 0.080 11 117762339 intron variant A/G snv 0.68 0.010 1.000 1 2011 2011
dbSNP: rs110402
rs110402
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
12 0.790 0.120 17 45802681 intron variant G/A;C snv 0.010 1.000 1 2014 2014
dbSNP: rs1116313
rs1116313
DRD2
1 1.000 0.080 11 113425385 intron variant A/G snv 0.45 0.010 1.000 1 2010 2010
dbSNP: rs1126671
rs1126671
ADH4 ; LOC100507053
5 0.851 0.120 4 99127263 missense variant T/C snv 0.76 0.75 0.010 1.000 1 2005 2005
dbSNP: rs1131445
rs1131445
IL16 ; STARD5
16 0.724 0.440 15 81309441 3 prime UTR variant T/A;C snv 0.010 1.000 1 2018 2018
dbSNP: rs1137070
rs1137070
MAOA
9 0.763 0.160 X 43744144 synonymous variant T/C snv 0.62 0.010 1.000 1 2017 2017
dbSNP: rs11568817
rs11568817
HTR1B ; LOC105377864
8 0.790 0.120 6 77463665 5 prime UTR variant A/C snv 0.37 0.010 1.000 1 2012 2012
dbSNP: rs11790959
rs11790959 		1 1.000 0.080 9 134127023 intergenic variant C/A;T snv 3.4E-03 0.010 1.000 1 2017 2017
dbSNP: rs12529
rs12529
AKR1C3
10 0.776 0.280 10 5094459 missense variant C/G snv 0.50 0.45 0.010 1.000 1 2011 2011
dbSNP: rs12597786
rs12597786
FTO
1 1.000 0.080 16 53787395 intron variant C/T snv 3.2E-02 0.010 1.000 1 2013 2013
dbSNP: rs130058
rs130058
HTR1B ; LOC105377864
8 0.790 0.120 6 77463564 5 prime UTR variant T/A;G snv 0.010 1.000 1 2012 2012
dbSNP: rs13212041
rs13212041
HTR1B ; LOC105377864
6 0.851 0.200 6 77461407 downstream gene variant C/T snv 0.70 0.010 1.000 1 2012 2012