Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1277073914
MUC12
0.925 0.040 7 100992117 missense variant T/A snv 2
rs11583043
DPH5
1.000 0.040 1 101000498 intron variant C/T snv 0.28 1
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 35
rs16910526
CLEC7A ; LOC105369655
0.742 0.280 12 10118488 stop gained A/C;G snv 6.2E-02 12
rs13107612
BANK1
0.827 0.120 4 101818823 intron variant C/T snv 0.31 5
rs4851529
LOC107985926
0.827 0.120 2 102030838 downstream gene variant G/A snv 0.44 5
rs10185424 0.925 0.040 2 102046427 intron variant T/G snv 0.62 2
rs2310173 0.925 0.080 2 102047167 intron variant T/C;G snv 2
rs871656
IL1R1
0.827 0.120 2 102154822 intron variant T/A;C snv 5
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs6543115
IL1RL1
1.000 0.040 2 102311181 upstream gene variant C/A;G snv 1
rs6543116
IL1RL1
0.882 0.120 2 102311266 upstream gene variant A/G snv 0.76 3
rs12987977
IL18R1
0.827 0.120 2 102358876 intron variant T/G snv 0.31 5
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 20
rs2075184 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 14
rs3740415
ACTR1A ; MFSD13A
1.000 0.040 10 102472959 3 prime UTR variant G/A snv 0.48 0.48 1
rs28362491
LOC105377621 ; NFKB1
0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs72696119
LOC105377621 ; NFKB1
0.925 0.120 4 102501347 5 prime UTR variant C/G snv 0.43 3
rs3774937
NFKB1
0.776 0.280 4 102513096 intron variant T/C snv 0.26 9
rs3774959
NFKB1
0.925 0.080 4 102589957 intron variant G/A snv 0.34 2
rs683878
WTAPP1
1.000 0.040 11 102834927 intron variant C/A;G snv 1
rs650108
MMP3
0.827 0.160 11 102838056 intron variant G/A snv 0.31 6
rs1799969
ICAM1
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 38
rs522616
MMP3
0.763 0.320 11 102844317 upstream gene variant T/C snv 0.23 10
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99