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: rs2682826
rs2682826
NOS1
11 0.807 0.280 12 117215033 3 prime UTR variant G/A snv 0.25 0.010 1.000 1 2010 2010
dbSNP: rs1217691063
rs1217691063
MTHFR
614 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.010 < 0.001 1 2012 2012
dbSNP: rs1801133
rs1801133
MTHFR
174 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 0.010 1.000 1 2012 2012
dbSNP: rs9393
rs9393
YWHAE
1 17 1345098 3 prime UTR variant A/G snv 0.12 0.010 1.000 1 2005 2005
dbSNP: rs3752826
rs3752826
YWHAE
1 17 1361770 non coding transcript exon variant A/C snv 0.75 0.010 1.000 1 2005 2005
dbSNP: rs1532976
rs1532976 		1 17 1405534 intergenic variant A/G snv 0.75 0.010 1.000 1 2005 2005
dbSNP: rs10416814
rs10416814
PTGER1
1 19 14476390 upstream gene variant T/A snv 0.33 0.010 1.000 1 2011 2011
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 2008 2012
dbSNP: rs181058279
rs181058279
SP110
1 2 230169144 missense variant C/G;T snv 3.8E-04; 2.4E-05 0.010 1.000 1 2018 2018
dbSNP: rs821616
rs821616
DISC1 ; TSNAX-DISC1
13 0.752 0.200 1 232008852 missense variant A/T snv 0.26 0.29 0.010 1.000 1 2014 2014
dbSNP: rs4307059
rs4307059 		5 0.882 0.080 5 25967594 intron variant T/A;C snv 0.010 1.000 1 2012 2012
dbSNP: rs7124442
rs7124442
BDNF ; BDNF-AS
9 0.827 0.160 11 27655494 3 prime UTR variant C/G;T snv 0.010 1.000 1 2015 2015
dbSNP: rs6265
rs6265
BDNF ; BDNF-AS
272 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.040 1.000 4 2012 2015
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 2013 2013
dbSNP: rs10767664
rs10767664
BDNF
16 0.752 0.400 11 27704439 intron variant T/A snv 0.83 0.010 1.000 1 2015 2015
dbSNP: rs962369
rs962369
BDNF
3 11 27712873 intron variant T/C snv 0.24 0.010 1.000 1 2015 2015
dbSNP: rs12273363
rs12273363
BDNF
11 0.807 0.120 11 27723312 intron variant T/C snv 0.16 0.010 1.000 1 2015 2015
dbSNP: rs908867
rs908867 		7 0.851 0.160 11 27724217 intron variant C/G;T snv 0.010 1.000 1 2015 2015
dbSNP: rs1491850
rs1491850 		6 0.925 0.080 11 27728178 intron variant T/C snv 0.37 0.010 1.000 1 2015 2015
dbSNP: rs1491851
rs1491851 		4 0.925 0.080 11 27731216 intron variant T/C;G snv 0.41 0.010 1.000 1 2015 2015
dbSNP: rs3800373
rs3800373
FKBP5 ; LOC101929309
22 0.752 0.200 6 35574699 3 prime UTR variant C/A snv 0.68 0.030 1.000 3 2011 2019
dbSNP: rs1360780
rs1360780
FKBP5 ; LOC112267956
31 0.708 0.320 6 35639794 intron variant T/A;C snv 0.020 1.000 2 2011 2019
dbSNP: rs76215382
rs76215382
AGBL2
1 11 47690268 missense variant A/G snv 1.2E-02 1.1E-02 0.010 1.000 1 2018 2018
dbSNP: rs121908538
rs121908538
SUCLA2
2 1.000 13 47954510 missense variant G/A snv 3.2E-05 1.4E-05 0.010 1.000 1 2018 2018
dbSNP: rs930752
rs930752
NRXN1
1 2 50109355 intron variant C/A snv 0.23 0.010 1.000 1 2012 2012