Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1321859
LOC105377891
0.925 0.080 6 90301954 intron variant C/T snv 0.24 2
rs28407950
HLA-DQB1-AS1
0.925 0.080 6 32658571 upstream gene variant C/T snv 0.29 2
rs58521088
BACH2
0.925 0.080 6 90275479 intron variant A/T snv 0.27 2
rs1800797
IL6 ; IL6-AS1 ; STEAP1B
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs4739738 0.882 0.120 8 80379410 intron variant G/A snv 0.60 3
rs35204956 0.925 0.080 8 80389778 intron variant A/-;AA;AAA delins 2
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 9
rs928413
IL33
0.807 0.120 9 6213387 upstream gene variant G/A;C snv 7
rs992969 0.882 0.080 9 6209697 intergenic variant A/G;T snv 4
rs62557312 0.925 0.080 9 6047765 intron variant C/T snv 0.15 2
rs12722502
IL2RA
0.882 0.080 10 6051176 intron variant C/T snv 7.8E-03 4
rs1775554 0.882 0.080 10 9012377 intergenic variant A/C snv 0.35 3
rs10795672 0.925 0.080 10 8735677 intergenic variant G/A;T snv 2
rs11255504
GATA3
0.925 0.080 10 8062378 intron variant A/G;T snv 2
rs7099257 0.925 0.080 10 8468994 upstream gene variant T/A snv 0.49 2
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 19
rs7936312 0.882 0.080 11 76582682 intergenic variant G/T snv 0.44 5
rs174621
FADS2
1.000 11 61862632 non coding transcript exon variant G/A;C snv 2
rs1784775
SIK2
0.925 0.080 11 111601736 upstream gene variant T/C snv 0.59 2
rs28415845 0.925 0.080 11 1151933 regulatory region variant T/C snv 0.58 2
rs12788104 1.000 11 1129831 regulatory region variant A/G snv 0.55 1
rs1059513
NAB2 ; STAT6
0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 11
rs7302200 0.851 0.200 12 56055651 regulatory region variant G/A snv 0.23 6
rs705699
SUOX ; RAB5B
0.882 0.160 12 55991020 non coding transcript exon variant G/A snv 0.40 5
rs3122929
STAT6
0.882 0.080 12 57115319 intron variant C/T snv 0.33 4