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: 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: 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: rs10196867
rs10196867
CTNNA2
5 0.925 0.080 2 79751234 intron variant C/G;T snv 0.710 1.000 1 2019 2019
dbSNP: rs10198241
rs10198241 		4 0.925 0.080 2 226115660 intergenic variant T/C snv 0.58 0.700 1.000 1 2017 2017
dbSNP: rs10211296
rs10211296
CSRNP3
3 1.000 0.080 2 165633833 intron variant A/G snv 0.34 0.700 1.000 1 2017 2017
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: rs10392
rs10392
PPP1R16B
6 0.882 0.160 20 38922292 3 prime UTR variant G/A snv 0.17 0.700 1.000 1 2017 2017
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: 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: rs10483038
rs10483038
KCNJ6
3 1.000 0.080 21 37652469 intron variant T/C snv 0.26 0.700 1.000 1 2012 2012
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: rs1057302
rs1057302
KIAA0040
1 1.000 0.080 1 175157287 3 prime UTR variant A/G snv 0.38 0.700 1.000 1 2011 2011
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: 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