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: rs11022778
rs11022778
ARNTL
6 0.925 0.080 11 13369313 intron variant T/A;G snv 0.010 1.000 1 2014 2014
dbSNP: rs11030101
rs11030101
BDNF ; BDNF-AS
10 0.763 0.160 11 27659197 5 prime UTR variant A/T snv 0.36 0.010 1.000 1 2013 2013
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 2015 2015
dbSNP: rs1106634
rs1106634
ATP6V1B2
5 0.851 0.080 8 20208538 intron variant G/A;C;T snv 0.18 0.010 1.000 1 2016 2016
dbSNP: rs11111
rs11111
GDNF ; GDNF-AS1
5 0.882 0.080 5 37814000 3 prime UTR variant T/C snv 0.22 0.010 1.000 1 2013 2013
dbSNP: rs112025902
rs112025902 		4 0.925 0.080 4 120232669 intron variant A/G;T snv 0.010 1.000 1 2016 2016
dbSNP: rs11240
rs11240
CLOCK ; TMEM165
2 0.925 0.080 4 55453183 3 prime UTR variant C/A;G snv 0.010 1.000 1 2015 2015
dbSNP: rs1130214
rs1130214
AKT1
12 0.742 0.280 14 104793397 5 prime UTR variant C/A snv 0.31 0.020 1.000 2 2016 2018
dbSNP: rs1130864
rs1130864
CRP
27 0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 0.020 0.500 2 2009 2015
dbSNP: rs1131691771
rs1131691771
PHIP ; IRAK1BP1
18 0.807 0.160 6 78958469 splice donor variant ACTT/- delins 0.700 0
dbSNP: rs115482041
rs115482041
RCL1
4 0.925 0.080 9 4860267 missense variant C/T snv 2.6E-03 2.3E-03 0.010 1.000 1 2018 2018
dbSNP: rs11636753
rs11636753
CHRNB4
4 0.882 0.120 15 78636604 intron variant G/T snv 0.35 0.010 1.000 1 2012 2012
dbSNP: rs1173546708
rs1173546708
TPH1
5 0.851 0.120 11 18040661 synonymous variant G/A snv 4.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs11754661
rs11754661
MTHFD1L
6 0.851 0.120 6 150885942 intron variant G/A;T snv 0.010 1.000 1 2016 2016
dbSNP: rs1176744
rs1176744
HTR3B
19 0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 0.010 1.000 1 2008 2008
dbSNP: rs11824092
rs11824092
ARNTL
7 0.925 0.080 11 13324747 intron variant T/C snv 0.62 0.010 1.000 1 2014 2014
dbSNP: rs1187323
rs1187323
NTRK2
5 0.882 0.080 9 84668501 upstream gene variant C/A;G;T snv 0.020 1.000 2 2009 2015
dbSNP: rs1187329
rs1187329
NTRK2
3 0.925 0.080 9 84674365 intron variant A/G snv 0.52 0.010 1.000 1 2009 2009
dbSNP: rs11904814
rs11904814
CREB1
5 0.851 0.080 2 207562074 intron variant T/G snv 0.30 0.010 1.000 1 2010 2010
dbSNP: rs11911834
rs11911834
S100B
4 0.882 0.080 21 46602608 5 prime UTR variant G/A;T snv 0.010 1.000 1 2009 2009
dbSNP: rs11932595
rs11932595
CLOCK
12 0.827 0.160 4 55457430 intron variant A/G;T snv 0.020 1.000 2 2014 2019
dbSNP: rs120074175
rs120074175
TPH2
7 0.827 0.080 12 72031544 missense variant G/A snv 1.2E-05 7.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs1202184
rs1202184
ABCB1
7 0.851 0.120 7 87584585 intron variant C/T snv 0.39 0.010 1.000 1 2011 2011
dbSNP: rs1205
rs1205
CRP
46 0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 0.040 1.000 4 2009 2018
dbSNP: rs1212171
rs1212171
NTRK2
8 0.851 0.120 9 84667612 upstream gene variant C/T snv 0.50 0.010 1.000 1 2013 2013