Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs61816761
FLG ; FLG-AS1
0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 43
rs4833095
TLR1
0.662 0.480 4 38798089 missense variant T/C snv 0.38 0.44 28
rs5743618
TLR1
0.677 0.360 4 38797027 missense variant C/A snv 0.53 0.51 25
rs5743810
TLR6 ; TLR1
0.689 0.360 4 38828729 missense variant A/G snv 0.73 0.72 21
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 18
rs7725052 0.716 0.240 5 40487168 intron variant C/T snv 0.52 16
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 16
rs7137828
ATXN2
0.763 0.200 12 111494996 intron variant C/A;T snv 15
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 14
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60 14
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 12
rs3939286 0.776 0.360 9 6210099 regulatory region variant T/A;C snv 12
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 12
rs8067378 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 12
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 12
rs550057
ABO
0.925 0.080 9 133271182 intron variant T/A;C snv 11
rs1143633
IL1B
0.752 0.280 2 112832890 intron variant C/G;T snv 11
rs1059513
NAB2 ; STAT6
0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 11
rs8076131
ORMDL3
0.790 0.200 17 39924659 intron variant G/A;C snv 11
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 10
rs11171739
ERBB3
0.807 0.320 12 56076841 5 prime UTR variant C/T snv 0.49 10
rs2305480
GSDMB
0.763 0.280 17 39905943 missense variant G/A snv 0.40 0.35 10