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: rs1075650
rs1075650
IER5L
1 9 129176634 3 prime UTR variant T/C snv 0.25 0.010 1.000 1 2015 2015
dbSNP: rs16918875
rs16918875
OPRK1
1 8 53229594 synonymous variant G/A snv 4.3E-02 7.1E-02 0.010 1.000 1 2012 2012
dbSNP: rs1875999
rs1875999
CRHBP
1 5 76969157 3 prime UTR variant T/C snv 0.38 0.010 1.000 1 2014 2014
dbSNP: rs2073837
rs2073837
DBH ; DBH-AS1
1 9 133657806 intron variant G/A snv 0.31 0.010 1.000 1 2018 2018
dbSNP: rs382140
rs382140 		1 7 108141755 intergenic variant A/G snv 0.74 0.010 1.000 1 2012 2012
dbSNP: rs7118900
rs7118900
ANKK1
1 11 113396099 missense variant G/A snv 0.25 0.25 0.010 1.000 1 2011 2011
dbSNP: rs772527880
rs772527880
AGFG1
1 2 227531108 missense variant G/A snv 4.0E-06 0.010 1.000 1 2011 2011
dbSNP: rs963549
rs963549
OPRK1
1 8 53229264 synonymous variant C/T snv 0.17 0.24 0.010 1.000 1 2012 2012
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: rs12043259
rs12043259
NFASC
2 1 204858913 intron variant C/G snv 0.11 0.700 1.000 1 2013 2013
dbSNP: rs1212415280
rs1212415280
VEGFA
2 6 43771130 missense variant G/T snv 2.1E-05 0.010 1.000 1 2019 2019
dbSNP: rs1409568
rs1409568 		2 1.000 0.040 10 118871273 intron variant T/C snv 8.2E-02 0.010 1.000 1 2018 2018
dbSNP: rs17228602
rs17228602
ACHE ; UFSP1
2 7 100890786 3 prime UTR variant C/T snv 1.5E-02 0.010 1.000 1 2019 2019
dbSNP: rs17664708
rs17664708
NRG1
2 1.000 0.080 8 32579499 intron variant C/T snv 1.0E-01 0.010 1.000 1 2012 2012
dbSNP: rs2377339
rs2377339
NCK2
2 2 105840835 intron variant A/G snv 4.8E-02 0.700 1.000 1 2013 2013
dbSNP: rs3025684
rs3025684
CREBBP
2 1.000 0.120 16 3745362 splice region variant G/A snv 7.7E-02 0.15 0.010 1.000 1 2011 2011
dbSNP: rs4648318
rs4648318
DRD2
2 1.000 0.080 11 113442667 intron variant T/C snv 0.33 0.010 1.000 1 2020 2020
dbSNP: rs764987358
rs764987358
ANGPT1
2 1.000 0.160 8 107347040 missense variant C/A snv 8.0E-06 1.4E-05 0.010 1.000 1 2019 2019
dbSNP: rs1040288
rs1040288
NR3C2
3 1.000 0.040 4 148126966 intron variant G/C snv 0.49 0.010 1.000 1 2014 2014
dbSNP: rs11030096
rs11030096
BDNF-AS
3 0.925 0.160 11 27643996 intron variant T/A;C snv 0.010 1.000 1 2016 2016
dbSNP: rs1611131
rs1611131
DBH ; DBH-AS1
3 0.925 0.080 9 133657065 splice region variant A/G snv 0.28; 4.0E-06 0.25 0.010 1.000 1 2018 2018
dbSNP: rs17228616
rs17228616
ACHE ; UFSP1
3 1.000 0.080 7 100890100 3 prime UTR variant G/T snv 9.8E-02 0.010 1.000 1 2019 2019
dbSNP: rs2180619
rs2180619
CNR1
3 1.000 0.040 6 88168233 upstream gene variant G/A snv 0.53 0.010 1.000 1 2014 2014
dbSNP: rs3495
rs3495
BCHE
3 0.925 0.160 3 165773193 3 prime UTR variant C/A;T snv 0.010 1.000 1 2019 2019
dbSNP: rs604300
rs604300
MGLL
3 1.000 0.080 3 127724009 intron variant A/G snv 0.91 0.010 1.000 1 2015 2015