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: rs16904179
rs16904179
CYRIB
1 1.000 0.040 8 129946705 intron variant G/A snv 6.2E-02 0.800 1.000 1 2013 2013
dbSNP: rs263232
rs263232
ADCY8
1 1.000 0.040 8 130795923 intron variant C/A snv 6.7E-02 0.800 1.000 1 2014 2014
dbSNP: rs406001
rs406001 		1 1.000 0.040 7 51938719 intergenic variant T/A;C snv 0.800 1.000 1 2013 2013
dbSNP: rs6812849
rs6812849
TLL1
1 1.000 0.040 4 165951384 intron variant C/A;T snv 0.800 1.000 1 2013 2013
dbSNP: rs682457
rs682457 		1 1.000 0.040 11 88216364 intergenic variant T/C snv 0.14 0.800 1.000 1 2014 2014
dbSNP: rs8042149
rs8042149
RORA
3 0.882 0.160 15 60832754 intron variant T/G snv 0.44 0.720 1.000 3 2013 2019
dbSNP: rs10170218
rs10170218 		1 1.000 0.040 2 187949717 intron variant A/C snv 0.25 0.700 1.000 1 2013 2013
dbSNP: rs1033962
rs1033962
PRTFDC1
1 1.000 0.040 10 24927877 intron variant C/T snv 0.33 0.700 1.000 1 2015 2015
dbSNP: rs159572
rs159572
ANKRD55
1 1.000 0.040 5 56211219 intron variant A/C snv 0.37 0.700 1.000 1 2016 2016
dbSNP: rs3100127
rs3100127 		1 1.000 0.040 1 202191842 upstream gene variant C/A;T snv 0.700 1.000 1 2015 2015
dbSNP: rs4511180
rs4511180
PTPRVP
1 1.000 0.040 1 202180311 non coding transcript exon variant A/G snv 0.65 0.700 1.000 1 2015 2015
dbSNP: rs4775301
rs4775301
RORA
2 0.925 0.040 15 60834660 intron variant T/C;G snv 0.700 1.000 1 2013 2013
dbSNP: rs58649573
rs58649573
LHX2
1 1.000 0.040 9 124005148 intron variant T/C snv 0.700 1.000 1 2015 2015
dbSNP: rs7691872
rs7691872
TLL1
1 1.000 0.040 4 165944433 intron variant G/C;T snv 0.700 1.000 1 2013 2013
dbSNP: rs7866350
rs7866350
TBC1D2
1 1.000 0.040 9 98221544 intron variant C/G;T snv 0.20 0.700 1.000 1 2015 2015
dbSNP: rs8024133
rs8024133
RORA
2 0.925 0.040 15 60838440 intron variant C/T snv 0.42 0.700 1.000 1 2013 2013
dbSNP: rs8041061
rs8041061
RORA
2 0.925 0.040 15 60832639 intron variant G/T snv 0.39 0.700 1.000 1 2013 2013
dbSNP: rs6265
rs6265
BDNF ; BDNF-AS
272 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.100 0.850 20 2006 2019
dbSNP: rs759834365
rs759834365
BDNF ; BDNF-AS
237 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 0.100 0.824 17 2006 2019
dbSNP: rs4680
rs4680
COMT ; MIR4761
249 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 0.080 0.750 8 2010 2019
dbSNP: rs1360780
rs1360780
FKBP5 ; LOC112267956
31 0.708 0.320 6 35639794 intron variant T/A;C snv 0.060 1.000 6 2013 2019
dbSNP: rs9470080
rs9470080
FKBP5
13 0.827 0.080 6 35678658 intron variant T/A;C snv 0.060 0.833 6 2008 2019
dbSNP: rs2267735
rs2267735
ADCYAP1R1
2 0.925 0.120 7 31095890 intron variant C/G snv 0.47 0.050 0.800 5 2013 2017
dbSNP: rs9296158
rs9296158
FKBP5 ; LOC112267956
16 0.763 0.080 6 35599305 intron variant A/G snv 0.65 0.050 0.800 5 2008 2019
dbSNP: rs11178997
rs11178997
TPH2
5 0.827 0.040 12 71938373 upstream gene variant T/A snv 0.12 0.030 0.667 3 2012 2019