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: rs224108
rs224108 		2 0.925 0.120 10 62789851 intron variant T/C;G snv 0.21 0.010 1.000 1 2019 2019
dbSNP: rs2918307
rs2918307 		1 1.000 0.120 19 8679458 downstream gene variant A/G;T snv 0.19 0.700 1.000 1 2015 2015
dbSNP: rs471144
rs471144 		1 1.000 0.120 1 152481779 intergenic variant T/G snv 8.0E-02 0.700 1.000 1 2015 2015
dbSNP: rs4982958
rs4982958 		4 0.851 0.200 14 24518659 intergenic variant C/T snv 0.50 0.010 1.000 1 2012 2012
dbSNP: rs5743399
rs5743399 		2 0.925 0.120 8 6880123 intron variant G/A snv 0.31 0.010 1.000 1 2009 2009
dbSNP: rs593982
rs593982 		1 1.000 0.120 11 65745636 upstream gene variant T/A;C snv 0.800 1.000 1 2012 2012
dbSNP: rs61813875
rs61813875 		1 1.000 0.120 1 152564174 downstream gene variant C/G snv 1.6E-02 0.700 1.000 1 2015 2015
dbSNP: rs6419573
rs6419573 		1 1.000 0.120 2 102410643 upstream gene variant T/C snv 0.78 0.700 1.000 1 2015 2015
dbSNP: rs6602364
rs6602364 		1 1.000 0.120 10 5996890 regulatory region variant G/C snv 0.50 0.700 1.000 1 2015 2015
dbSNP: rs6661961
rs6661961 		1 1.000 0.120 1 152469813 intergenic variant T/A;C snv 0.800 1.000 1 2013 2013
dbSNP: rs67766926
rs67766926 		2 0.925 0.120 2 60936446 downstream gene variant C/G snv 0.17 0.700 1.000 1 2015 2015
dbSNP: rs7000782
rs7000782 		1 1.000 0.120 8 80395915 intron variant T/A snv 0.54 0.800 1.000 1 2011 2011
dbSNP: rs712484
rs712484 		3 0.882 0.160 14 48081576 intergenic variant C/A snv 0.14 0.010 < 0.001 1 2012 2012
dbSNP: rs7124842
rs7124842 		3 0.882 0.160 11 76600576 intergenic variant G/A;C;T snv 0.010 1.000 1 2012 2012
dbSNP: rs7127307
rs7127307 		2 1.000 0.120 11 128317488 regulatory region variant T/C snv 0.47 0.700 1.000 1 2015 2015
dbSNP: rs7130588
rs7130588 		4 0.882 0.200 11 76559639 regulatory region variant A/G snv 0.29 0.800 1.000 1 2013 2013
dbSNP: rs7936562
rs7936562 		4 0.882 0.160 11 76567214 intergenic variant T/C snv 0.59 0.010 < 0.001 1 2012 2012
dbSNP: rs9302874
rs9302874 		2 0.925 0.120 17 78284479 intergenic variant C/T snv 0.24 0.700 1.000 1 2015 2015
dbSNP: rs976078
rs976078 		4 0.882 0.120 13 82963398 intron variant A/C snv 0.15 0.010 1.000 1 2018 2018
dbSNP: rs9952991
rs9952991 		2 0.925 0.120 18 12780465 upstream gene variant G/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs2853209
rs2853209
ADAM33
5 0.827 0.200 20 3670825 intron variant T/A snv 0.41 0.010 1.000 1 2009 2009
dbSNP: rs2066853
rs2066853
AHR
34 0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 0.010 1.000 1 2019 2019
dbSNP: rs10249788
rs10249788
AHR ; LOC101927609
6 0.827 0.160 7 17298523 intron variant C/G;T snv 0.010 1.000 1 2019 2019
dbSNP: rs1555525115
rs1555525115
ANKRD11
5 0.851 0.360 16 89279567 frameshift variant GGCTTCGG/- delins 0.700 0
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 2009 2009