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: rs4722999
rs4722999
CRHR2
5 0.851 0.080 7 30654159 intron variant C/T snv 0.67 0.010 1.000 1 2016 2016
dbSNP: rs7044343
rs7044343
IL33 ; LOC107987046
13 0.752 0.520 9 6254208 intron variant C/T snv 0.51 0.010 1.000 1 2016 2016
dbSNP: rs9829896
rs9829896
KAT2B ; MIR3135A
2 3 20135980 intron variant C/A;T snv 0.010 1.000 1 2016 2016
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 2017 2017
dbSNP: rs6265
rs6265
BDNF ; BDNF-AS
272 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.100 1.000 10 2005 2018
dbSNP: rs759834365
rs759834365
BDNF ; BDNF-AS
237 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 0.100 1.000 10 2005 2018
dbSNP: rs4680
rs4680
COMT ; MIR4761
249 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 0.030 1.000 3 2008 2018
dbSNP: rs1360780
rs1360780
FKBP5 ; LOC112267956
31 0.708 0.320 6 35639794 intron variant T/A;C snv 0.020 1.000 2 2011 2018
dbSNP: rs1800498
rs1800498
DRD2
4 0.882 0.080 11 113420866 intron variant G/A snv 0.44 0.010 1.000 1 2018 2018
dbSNP: rs678849
rs678849
OPRD1
5 0.882 0.120 1 28818676 intron variant C/T snv 0.44 0.010 1.000 1 2018 2018
dbSNP: rs9470080
rs9470080
FKBP5
13 0.827 0.080 6 35678658 intron variant T/A;C snv 0.030 1.000 3 2010 2019
dbSNP: rs1799971
rs1799971
OPRM1
95 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 0.020 1.000 2 2019 2019
dbSNP: rs53576
rs53576
CAV3 ; OXTR
42 0.641 0.320 3 8762685 intron variant A/G;T snv 0.010 1.000 1 2019 2019
dbSNP: rs56372821
rs56372821
EPHX2 ; GULOP
2 1.000 0.080 8 27578983 intron variant G/A snv 0.13 0.700 1.000 1 2019 2019