Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9372120
ATG5
0.851 0.280 6 106219660 intron variant T/G snv 0.16 5
rs10208293
IL1RL1 ; IL18R1
0.882 0.160 2 102349850 intron variant G/A snv 0.33 4
rs10414065 0.882 0.080 19 33230549 upstream gene variant C/T snv 5.5E-02 4
rs10494132
CHIA
0.851 0.080 1 111289601 upstream gene variant T/C snv 0.26 4
rs11071559
RORA
0.925 0.080 15 60777789 intron variant C/T snv 0.23 4
rs12123821
LOC112268240 ; FLG-AS1
0.925 0.080 1 152206676 intron variant C/T snv 2.9E-02 4
rs12413578 0.882 0.160 10 9007290 intergenic variant C/G;T snv 4
rs12722502
IL2RA
0.882 0.080 10 6051176 intron variant C/T snv 7.8E-03 4
rs143326447
MIR4435-2HG ; SOCAR
0.925 0.080 2 111511155 intron variant T/C snv 0.11 4
rs17144046 0.882 0.120 10 8564051 intergenic variant A/G snv 0.28 4
rs1999071 0.851 0.080 14 22659998 regulatory region variant T/C snv 0.29 4
rs2070901
FCER1G
0.882 0.120 1 161215268 non coding transcript exon variant G/T snv 0.32 4
rs2787094
ADAM33
0.851 0.160 20 3668514 3 prime UTR variant C/G snv 0.71 4
rs3122929
STAT6
0.882 0.080 12 57115319 intron variant C/T snv 0.33 4
rs3749833
IRF1-AS1
0.925 0.080 5 132463934 non coding transcript exon variant T/C snv 0.23 4
rs4574025
TNFRSF11A
0.882 0.160 18 62342581 intron variant C/T snv 0.55 4
rs61894547
EMSY
0.882 0.160 11 76537586 intron variant C/T snv 3.1E-02 4
rs6594499 0.882 0.120 5 111134439 downstream gene variant C/A snv 0.56 4
rs7219923
GSDMB
0.882 0.160 17 39918265 non coding transcript exon variant C/T snv 0.52 4
rs72823641
IL1RL1 ; IL18R1
0.882 0.080 2 102319699 intron variant T/A;C snv 4
rs8069176 0.882 0.080 17 39900944 downstream gene variant G/A;T snv 4
rs9303281
GSDMB
0.882 0.160 17 39917793 non coding transcript exon variant G/A snv 0.50 4
rs9357733
EFHC1
0.851 0.160 6 52427338 intron variant A/G snv 0.19 4
rs9391997
IRF4
0.851 0.160 6 409119 3 prime UTR variant A/G snv 0.38 4
rs9901146 0.882 0.160 17 39887090 intergenic variant G/A snv 0.45 4