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: rs2236857
rs2236857
OPRD1
1 1.000 0.080 1 28835097 intron variant T/C snv 0.28 0.020 1.000 2 2014 2019
dbSNP: rs10078866
rs10078866
DRD1
2 1.000 0.080 5 175445317 upstream gene variant A/G snv 5.2E-02 0.010 1.000 1 2015 2015
dbSNP: rs10494334
rs10494334 		1 1.000 0.080 1 163535374 intergenic variant G/A snv 0.10 0.010 1.000 1 2010 2010
dbSNP: rs1122079
rs1122079
RGS9
1 1.000 0.080 17 65218385 intron variant A/C;T snv 0.010 1.000 1 2015 2015
dbSNP: rs11503014
rs11503014
GABRA2
2 1.000 0.080 4 46388848 5 prime UTR variant C/G snv 0.27 0.010 1.000 1 2010 2010
dbSNP: rs11606194
rs11606194
HTR3B
1 1.000 0.080 11 113910259 intron variant T/C snv 6.1E-02 0.010 1.000 1 2015 2015
dbSNP: rs1650420
rs1650420
GRIN2A
2 1.000 0.080 16 10174473 intron variant T/C snv 0.58 0.010 1.000 1 2013 2013
dbSNP: rs1714984
rs1714984
MYOCD
1 1.000 0.080 17 12714384 intron variant A/G;T snv 0.010 1.000 1 2008 2008
dbSNP: rs17189632
rs17189632
GRIN3A
1 1.000 0.080 9 101605720 intron variant T/A snv 0.41 0.010 1.000 1 2016 2016
dbSNP: rs1867898
rs1867898 		1 1.000 0.080 2 133762000 intergenic variant G/A snv 0.22 0.010 1.000 1 2008 2008
dbSNP: rs1978340
rs1978340
GAD1
1 1.000 0.080 2 170813611 non coding transcript exon variant G/A snv 0.25 0.010 1.000 1 2012 2012
dbSNP: rs1986513
rs1986513 		1 1.000 0.080 4 125146073 intergenic variant A/T snv 8.9E-02 0.010 1.000 1 2008 2008
dbSNP: rs1997644
rs1997644
CSNK1E ; TPTEP2-CSNK1E
1 1.000 0.080 22 38319217 intron variant G/A snv 0.44 0.010 1.000 1 2014 2014
dbSNP: rs2270162
rs2270162
AUTS2 ; CT66
1 1.000 0.080 7 69596980 intron variant C/G;T snv 0.010 1.000 1 2014 2014
dbSNP: rs2288156
rs2288156
CCDC42
1 1.000 0.080 17 8741536 missense variant C/A;T snv 4.0E-06; 8.8E-02 0.700 1.000 1 2016 2016
dbSNP: rs2292592
rs2292592
RGS9
1 1.000 0.080 17 65208091 intron variant A/G snv 0.12 0.010 1.000 1 2015 2015
dbSNP: rs2292593
rs2292593
RGS9
1 1.000 0.080 17 65201802 intron variant T/C snv 0.20 0.010 1.000 1 2015 2015
dbSNP: rs255105
rs255105
CRHR2
1 1.000 0.080 7 30692491 intron variant T/C snv 0.50 0.010 1.000 1 2018 2018
dbSNP: rs274618
rs274618
GRM3
1 1.000 0.080 7 86642700 upstream gene variant T/A;C snv 0.010 1.000 1 2014 2014
dbSNP: rs2869577
rs2869577
RGS9
1 1.000 0.080 17 65199474 intron variant C/G snv 0.12 0.010 1.000 1 2015 2015
dbSNP: rs3104703
rs3104703
GRIN2A
1 1.000 0.080 16 9971279 intron variant T/G snv 0.48 0.010 1.000 1 2013 2013
dbSNP: rs3219790
rs3219790
GRIN2A
1 1.000 0.080 16 10183568 upstream gene variant CACACACACACACACACA/-;CA;CACA;CACACA;CACACACA;CACACACACA;CACACACACACA;CACACACACACACA;CACACACACACACACA;CACACACACACACACACACA;CACACACACACACACACACACA;CACACACACACACACACACACACA;CACACACACACACACACACACACACA;CACACACACACACACACACACACACACA;CACACACACACACACACACACACACACACA;CACACACACACACACACACACACACACACACA;CACACACACACACACACACACACACACACACACA;CACACACACACACACACACACACACACACACACACA;CACACACACACACACACACACACACACACACACACACA;CACACACACACACACACACACACACACACACACACACACA;CACACACACACACACACACACACACACACACACACACACACA delins 0.010 1.000 1 2013 2013
dbSNP: rs363332
rs363332
SLC18A2 ; LOC105378500
1 1.000 0.080 10 117243156 intron variant G/A snv 0.18 0.010 1.000 1 2019 2019
dbSNP: rs363334
rs363334
SLC18A2
1 1.000 0.080 10 117245484 intron variant C/G snv 0.25 0.010 1.000 1 2019 2019
dbSNP: rs363338
rs363338
SLC18A2
1 1.000 0.080 10 117249878 intron variant C/T snv 0.58 0.010 1.000 1 2019 2019