Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs67766926 0.925 0.120 2 60936446 downstream gene variant C/G snv 0.17 2
rs7127307 1.000 0.120 11 128317488 regulatory region variant T/C snv 0.47 2
rs9302874 0.925 0.120 17 78284479 intergenic variant C/T snv 0.24 2
rs9952991 0.925 0.120 18 12780465 upstream gene variant G/A;C snv 2
rs10214237 1.000 0.120 5 35883632 downstream gene variant T/C snv 0.21 1
rs10738626 1.000 0.120 9 22373458 intergenic variant C/G;T snv 1
rs10888499 1.000 0.120 1 152560266 intergenic variant C/A;T snv 1
rs11205006 1.000 0.120 1 152467700 intergenic variant A/T snv 0.72 1
rs12144049 1.000 0.120 1 152468434 intergenic variant C/G;T snv 1
rs1444418 1.000 0.120 10 62800710 intron variant A/G snv 0.22 1
rs16999165 1.000 0.120 20 54190682 intergenic variant A/G snv 5.5E-02 1
rs2212434 1.000 0.120 11 76570549 intergenic variant C/T snv 0.39 1
rs2918307 1.000 0.120 19 8679458 downstream gene variant A/G;T snv 0.19 1
rs471144 1.000 0.120 1 152481779 intergenic variant T/G snv 8.0E-02 1
rs593982 1.000 0.120 11 65745636 upstream gene variant T/A;C snv 1
rs61813875 1.000 0.120 1 152564174 downstream gene variant C/G snv 1.6E-02 1
rs6419573 1.000 0.120 2 102410643 upstream gene variant T/C snv 0.78 1
rs6602364 1.000 0.120 10 5996890 regulatory region variant G/C snv 0.50 1
rs6661961 1.000 0.120 1 152469813 intergenic variant T/A;C snv 1
rs7000782 1.000 0.120 8 80395915 intron variant T/A snv 0.54 1
rs2853209
ADAM33
0.827 0.200 20 3670825 intron variant T/A snv 0.41 5
rs2066853
AHR
0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 34
rs1555525115
ANKRD11
0.851 0.360 16 89279567 frameshift variant GGCTTCGG/- delins 5
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272