Disease: Autoimmune Diseases
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1036199
HAVCR2
0.925 0.160 5 157104725 missense variant C/A snv 0.87 0.83 3
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 13
rs104895271
TNFRSF1A
0.851 0.240 12 6334161 missense variant A/C;G snv 1.6E-04; 4.8E-05 6
rs1050501
FCGR2B
0.732 0.440 1 161674008 missense variant T/C snv 0.16 0.19 15
rs10516487
BANK1
0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 11
rs1059702
IRAK1
0.807 0.280 X 154018741 missense variant A/G snv 0.72 7
rs1059703
IRAK1
0.851 0.280 X 154013378 missense variant G/A snv 0.67 6
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs10892279 1.000 0.120 11 118741072 intron variant G/A;T snv 0.25 3
rs10954213
IRF5
0.752 0.200 7 128949373 3 prime UTR variant G/A snv 0.58 11
rs11203203
UBASH3A
0.807 0.240 21 42416077 intron variant G/A snv 0.28 9
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs1126407
LOC107985367 ; LGALS8
0.925 0.200 1 236537507 missense variant T/A snv 0.61 0.61 3
rs11264799
FCRL3
0.851 0.240 1 157700967 upstream gene variant C/T snv 0.28 6
rs1143679
ITGAM
0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 14
rs11586238 0.925 0.160 1 116720516 regulatory region variant C/G snv 0.19 4
rs11676922
AFF3
0.925 0.160 2 100190478 intron variant T/A snv 0.51 4
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs13031237
REL
1.000 0.120 2 60908994 intron variant G/T snv 0.25 3
rs1310182
AP4B1-AS1 ; PTPN22
0.882 0.360 1 113830881 intron variant A/C;G snv 0.56 4
rs13119723
KIAA1109
0.807 0.280 4 122297158 intron variant A/G snv 0.10 8
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs13315591
FAM107A ; LOC107984079
0.925 0.160 3 58571114 intron variant T/C snv 0.15 4
rs13447
NCF1C
0.882 0.200 7 75166663 non coding transcript exon variant T/A;C snv 1.9E-02 4