Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
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
rs280519
TYK2
0.752 0.320 19 10362257 splice region variant A/C;G snv 0.50 10
rs2304256
TYK2
0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 13
rs11879191
CDC37
1.000 0.040 19 10402235 intron variant G/A;C snv 2
rs62131887 0.724 0.240 19 10476920 intergenic variant C/T snv 0.37 14
rs1239681664
ABCA1
0.716 0.320 9 104818690 synonymous variant A/G snv 7.0E-06 15
rs35074907
KEAP1
0.807 0.160 19 10489742 synonymous variant G/A snv 1.9E-02 1.5E-02 6
rs11750385
LINC02213
0.827 0.120 5 10521556 intron variant G/A;T snv 5
rs6568421 1.000 0.040 6 105987150 regulatory region variant A/G snv 0.23 2
rs7746082 0.851 0.160 6 105987394 regulatory region variant G/A;C 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
rs12014762
MORC4
0.882 0.080 X 106940440 intron variant C/T snv 0.14 3
rs2930047
DAP
0.925 0.040 5 10695414 intron variant T/C snv 0.49 3
rs6622126
MORC4
0.851 0.080 X 106956972 missense variant G/A snv 0.58 4
rs878859113
CD24
0.763 0.360 6 106971734 missense variant G/A snv 0.35 11
rs11825977
MUC2
0.925 0.040 11 1075920 splice region variant G/A snv 0.18 0.20 2
rs7805114 0.827 0.120 7 107809588 downstream gene variant T/A;G snv 5
rs6466198 0.827 0.120 7 107839681 regulatory region variant A/T snv 0.68 5