Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7848647
TNFSF15
0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74 13
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs72556554
ATRIP ; TREX1 ; ATRIP-TREX1
0.776 0.400 3 48466996 missense variant G/A;C snv 2.1E-04; 2.7E-04 9
rs5029939
TNFAIP3
0.701 0.440 6 137874586 intron variant C/G snv 0.13 19
rs3813946
CR2
0.827 0.280 1 207454348 5 prime UTR variant T/C snv 0.16 5
rs3810936
TNFSF15
0.742 0.320 9 114790605 synonymous variant T/C snv 0.71 0.75 12
rs370504038
ATRIP-TREX1 ; ATRIP ; SHISA5 ; TREX1
0.851 0.160 3 48467569 missense variant A/G snv 1.2E-04 1.2E-04 4
rs3131379
MSH5 ; MSH5-SAPCD1
0.752 0.440 6 31753256 intron variant G/A snv 6.4E-02 7.9E-02 10
rs3093061
CRP
0.851 0.160 1 159715192 upstream gene variant T/C snv 4.8E-02 4
rs292001
C1QA
0.807 0.320 1 22638465 intron variant G/A snv 0.54 6
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs2397084
IL17F
0.716 0.480 6 52237046 missense variant T/C snv 6.7E-02 6.1E-02 14
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs2205960
TNFSF4
0.763 0.400 1 173222336 intergenic variant G/A;T snv 9
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs2070197
IRF5
0.827 0.280 7 128948946 3 prime UTR variant T/C snv 9.0E-02 6
rs2004640
IRF5
0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26
rs1980422 0.776 0.320 2 203745673 intergenic variant C/A;T snv 9
rs1876453
CR2
0.851 0.160 1 207454573 intron variant G/A snv 8.4E-02 4
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs17615
CR2
0.827 0.200 1 207473117 missense variant G/A snv 0.26 0.31 5
rs1678542
KIF5A
0.790 0.320 12 57574932 intron variant C/G snv 0.42 9