Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs763362
CD226
1.000 0.080 18 69864561 intron variant A/G snv 0.37 1
rs34481144
IFITM3
1.000 0.080 11 320836 5 prime UTR variant C/T snv 0.36 0.34 1
rs8072510
SLFN13
1.000 0.080 17 35445639 stop gained G/T snv 9.5E-02 9.9E-02 1
rs1048479
ST3GAL1
1.000 0.080 8 133461905 synonymous variant C/T snv 0.51 0.47 1
rs113350588
ST3GAL1
1.000 0.080 8 133475740 synonymous variant G/A snv 1.6E-04 1.8E-04 1
rs9271117
HLA-DRB1
0.925 0.160 6 32609018 intergenic variant C/T snv 0.72 2
rs1468575151
PBRM1
0.925 0.080 3 52668520 missense variant T/C snv 7.0E-06 2
rs773340854
GALNS ; LOC107987238
0.882 0.200 16 88824828 missense variant G/A snv 4.0E-06 3
rs7744020
HLA-DQB1-AS1
0.882 0.160 6 32658353 upstream gene variant G/A snv 0.34 3
rs2229291
CPT2
0.827 0.200 1 53210729 missense variant T/G snv 2.3E-02 1.5E-02 8
rs12252
IFITM3
0.695 0.240 11 320772 splice region variant A/G snv 0.13 0.13 23
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182