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: rs1217691063
rs1217691063
MTHFR
614 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.010 1.000 1 2015 2015
dbSNP: rs562010289
rs562010289
LAMC2
2 0.925 0.120 1 183227583 missense variant G/A;C snv 1.7E-04 0.010 1.000 1 2010 2010
dbSNP: rs11127292
rs11127292
MYT1L
2 0.925 0.160 2 2026171 intron variant C/T snv 0.11 0.010 1.000 1 2014 2014
dbSNP: rs3771863
rs3771863
TACR1 ; LOC105374811
2 0.925 0.240 2 75192588 intron variant C/T snv 0.30 0.010 1.000 1 2015 2015
dbSNP: rs1043210477
rs1043210477
GPX1
19 0.701 0.520 3 49358250 missense variant G/A snv 0.010 < 0.001 1 2014 2014
dbSNP: rs6280
rs6280
DRD3
57 0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 0.010 1.000 1 2009 2009
dbSNP: rs1126858
rs1126858
ART3 ; CXCL10
1 1.000 0.080 4 76021932 stop lost A/G snv 2.9E-04 2.4E-04 0.010 1.000 1 2013 2013
dbSNP: rs5522
rs5522
NR3C2
19 0.732 0.320 4 148436323 missense variant C/T snv 0.88 0.89 0.010 1.000 1 2008 2008
dbSNP: rs375382379
rs375382379
NR3C1
5 0.882 0.160 5 143399792 missense variant T/C snv 4.0E-06 0.010 1.000 1 2008 2008
dbSNP: rs550659379
rs550659379
NR3C1
5 0.882 0.160 5 143399780 missense variant T/C snv 4.0E-06 7.0E-06 0.010 1.000 1 2008 2008
dbSNP: rs752834812
rs752834812
NR3C1
5 0.882 0.160 5 143399885 missense variant T/C snv 8.0E-06 0.010 1.000 1 2008 2008
dbSNP: rs772651364
rs772651364
NR3C1
5 0.882 0.160 5 143400050 missense variant C/T snv 4.0E-06 0.010 1.000 1 2008 2008
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 2014 2018
dbSNP: rs1800541
rs1800541
EDN1
5 0.851 0.120 6 12288986 upstream gene variant T/G snv 0.24 0.010 1.000 1 2017 2017
dbSNP: rs1314305899
rs1314305899
NOS3
6 0.807 0.280 7 151003224 missense variant C/T snv 7.9E-06 2.1E-05 0.010 1.000 1 2015 2015
dbSNP: rs1799983
rs1799983
NOS3
246 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2007 2007
dbSNP: rs2097903
rs2097903
MGC4859 ; LOC107986766
1 1.000 0.080 7 10642782 intron variant A/T snv 0.51 0.010 1.000 1 2018 2018
dbSNP: rs1048101
rs1048101
ADRA1A
5 0.882 0.120 8 26770511 missense variant A/G snv 0.52 0.56 0.010 1.000 1 2009 2009
dbSNP: rs1383914
rs1383914
ADRA1A
1 1.000 0.080 8 26865532 5 prime UTR variant T/C snv 0.47 0.010 1.000 1 2009 2009
dbSNP: rs11030104
rs11030104
BDNF ; BDNF-AS
12 0.790 0.240 11 27662970 intron variant A/G snv 0.16 0.010 1.000 1 2018 2018
dbSNP: rs12273539
rs12273539
BDNF ; BDNF-AS
2 0.925 0.120 11 27661764 intron variant C/T snv 0.12 0.010 1.000 1 2018 2018
dbSNP: rs6265
rs6265
BDNF ; BDNF-AS
272 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.010 1.000 1 2012 2012
dbSNP: rs759834365
rs759834365
BDNF ; BDNF-AS
237 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 0.010 1.000 1 2012 2012
dbSNP: rs79448530
rs79448530
C11orf40
1 1.000 0.080 11 4577726 non coding transcript exon variant C/G;T snv 4.0E-06; 3.7E-02 0.010 1.000 1 2013 2013
dbSNP: rs6313
rs6313
HTR2A
82 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 0.050 0.600 5 1999 2012