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: rs1006737
rs1006737
CACNA1C
27 0.695 0.120 12 2236129 intron variant G/A snv 0.36 0.070 1.000 7 2010 2014
dbSNP: rs6295
rs6295
HTR1A
40 0.645 0.200 5 63962738 intron variant C/G snv 0.49 0.050 1.000 5 2009 2017
dbSNP: rs6311
rs6311
HTR2A
41 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.050 1.000 5 2010 2019
dbSNP: rs1360780
rs1360780
FKBP5 ; LOC112267956
31 0.708 0.320 6 35639794 intron variant T/A;C snv 0.030 1.000 3 2014 2019
dbSNP: rs11030101
rs11030101
BDNF ; BDNF-AS
10 0.763 0.160 11 27659197 5 prime UTR variant A/T snv 0.36 0.020 1.000 2 2012 2013
dbSNP: rs1800532
rs1800532
TPH1
15 0.763 0.160 11 18026269 intron variant G/T snv 0.33 0.020 1.000 2 2012 2019
dbSNP: rs2242446
rs2242446
SLC6A2
9 0.776 0.080 16 55656513 5 prime UTR variant C/A;T snv 0.020 1.000 2 2008 2017
dbSNP: rs25531
rs25531
SLC6A4 ; LOC105371720
72 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 0.020 1.000 2 2012 2019
dbSNP: rs334558
rs334558
GSK3B ; LOC107986119
20 0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51 0.020 1.000 2 2017 2019
dbSNP: rs397507444
rs397507444
MTHFR
306 0.405 0.880 1 11794407 missense variant T/G snv 0.020 1.000 2 2012 2017
dbSNP: rs40184
rs40184
SLC6A3
5 0.851 0.120 5 1394962 intron variant C/T snv 0.45 0.020 1.000 2 2008 2010
dbSNP: rs10233018
rs10233018 		2 0.925 0.040 7 117883655 non coding transcript exon variant A/G snv 0.53 0.700 1.000 1 2016 2016
dbSNP: rs10405744
rs10405744
ZNF93
4 0.851 0.040 19 19948684 intron variant G/A snv 9.0E-02 0.700 1.000 1 2015 2015
dbSNP: rs10447760
rs10447760 		4 0.851 0.040 7 114083210 upstream gene variant C/T snv 0.17 0.010 1.000 1 2013 2013
dbSNP: rs10485715
rs10485715 		2 0.925 0.040 20 7279278 intergenic variant T/C snv 5.5E-02 0.700 1.000 1 2016 2016
dbSNP: rs10494251
rs10494251
BCL9
4 0.851 0.040 1 147552120 intron variant C/T snv 5.8E-02 0.010 1.000 1 2011 2011
dbSNP: rs10514299
rs10514299
TMEM161B-AS1
6 0.827 0.120 5 88367793 intron variant C/T snv 0.21 0.010 1.000 1 2018 2018
dbSNP: rs10748842
rs10748842
NRG3
8 0.807 0.120 10 81889983 intron variant T/C snv 0.13 0.010 1.000 1 2017 2017
dbSNP: rs10809520
rs10809520 		2 0.925 0.040 9 11557797 intergenic variant C/T snv 0.28 0.700 1.000 1 2016 2016
dbSNP: rs10884216
rs10884216
LINC02627
2 0.925 0.040 10 105701367 intergenic variant T/C snv 0.17 0.700 1.000 1 2016 2016
dbSNP: rs10968749
rs10968749
LINGO2
4 0.851 0.040 9 28752486 intergenic variant A/G snv 5.5E-02 0.700 1.000 1 2015 2015
dbSNP: rs10994336
rs10994336
ANK3
12 0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 0.010 1.000 1 2011 2011
dbSNP: rs11082011
rs11082011
CELF4
3 0.925 0.040 18 37565159 intron variant C/T snv 0.53 0.700 1.000 1 2018 2018
dbSNP: rs111365677
rs111365677 		3 0.925 0.040 1 99463578 upstream gene variant T/C snv 2.3E-03 0.700 1.000 1 2016 2016
dbSNP: rs11155372
rs11155372
UTRN
3 0.925 0.040 6 144698602 intron variant G/C;T snv 0.700 1.000 1 2018 2018