Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107612
BANK1
0.827 0.120 4 101818823 intron variant C/T snv 0.31 5
rs2302589
IL1R2
1.000 0.040 2 102008324 intron variant C/T snv 0.17 1
rs4851529
LOC107985926
0.827 0.120 2 102030838 downstream gene variant G/A snv 0.44 5
rs2310173 0.925 0.080 2 102047167 intron variant T/C;G snv 2
rs2234650
IL1R1
0.925 0.080 2 102141867 5 prime UTR variant C/G;T snv 2
rs871656
IL1R1
0.827 0.120 2 102154822 intron variant T/A;C snv 5
rs12987977
IL18R1
0.827 0.120 2 102358876 intron variant T/G snv 0.31 5
rs2075184 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 14
rs3774937
NFKB1
0.776 0.280 4 102513096 intron variant T/C snv 0.26 9
rs3740938
MMP8
1.000 0.040 11 102716331 synonymous variant G/A snv 9.7E-02 6.3E-02 1
rs142481975
MMP3
1.000 0.040 11 102843480 missense variant C/T snv 4.0E-06 1
rs522616
MMP3
0.763 0.320 11 102844317 upstream gene variant T/C snv 0.23 10
rs74956615
FDX2 ; RAVER1
0.807 0.160 19 10317045 3 prime UTR variant T/A;C snv 6
rs35018800
TYK2
0.790 0.160 19 10354167 missense variant G/A snv 4.6E-03 4.9E-03 9
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 12
rs35164067
CDC37
1.000 0.040 19 10414505 intron variant G/A snv 0.18 2
rs62131887 0.724 0.240 19 10476920 intergenic variant C/T snv 0.37 14
rs35074907
KEAP1
0.807 0.160 19 10489742 synonymous variant G/A snv 1.9E-02 1.5E-02 6
rs2841277
PLD4
0.882 0.120 14 104924668 upstream gene variant C/T snv 0.41 3
rs11750385
LINC02213
0.827 0.120 5 10521556 intron variant G/A;T snv 5
rs4946717
PRDM1
0.827 0.120 6 106026874 intron variant C/A;G;T snv 6
rs28701841
ATG5 ; PRDM1
0.827 0.120 6 106082455 intron variant G/A snv 7.6E-02 5
rs11839053 0.724 0.240 13 106410694 intergenic variant T/C snv 7.0E-02 14
rs12369214
RIC8B
0.807 0.120 12 106804833 intron variant G/A snv 0.41 6
rs3776414
DAP
0.827 0.120 5 10689450 intron variant T/G snv 0.48 6