Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1341239
PRL ; CASC15
0.776 0.360 6 22303975 intron variant A/C snv 0.65 8
rs10489265
TNFSF4 ; LOC100506023
0.827 0.200 1 173266926 regulatory region variant A/C snv 0.21 5
rs1518110
IL10 ; IL19
0.851 0.160 1 206771516 intron variant A/C;T snv 5
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs1270942
CFB ; CYP21A2
0.742 0.440 6 31951083 non coding transcript exon variant A/G snv 7.5E-02 11
rs12938
C1orf112 ; SELL
0.851 0.160 1 169691640 3 prime UTR variant A/G snv 0.27 5
rs370504038
ATRIP-TREX1 ; ATRIP ; SHISA5 ; TREX1
0.851 0.160 3 48467569 missense variant A/G snv 1.2E-04 1.2E-04 4
rs1980422 0.776 0.320 2 203745673 intergenic variant C/A;T snv 9
rs5029939
TNFAIP3
0.701 0.440 6 137874586 intron variant C/G snv 0.13 19
rs1678542
KIF5A
0.790 0.320 12 57574932 intron variant C/G snv 0.42 9
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 27
rs121908117
ATRIP ; TREX1 ; ATRIP-TREX1
0.708 0.440 3 48466707 missense variant G/A snv 17
rs1143679
ITGAM
0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 14
rs3131379
MSH5 ; MSH5-SAPCD1
0.752 0.440 6 31753256 intron variant G/A snv 6.4E-02 7.9E-02 10
rs292001
C1QA
0.807 0.320 1 22638465 intron variant G/A snv 0.54 6
rs17615
CR2
0.827 0.200 1 207473117 missense variant G/A snv 0.26 0.31 5
rs13023380
IFIH1
0.851 0.160 2 162297853 intron variant G/A snv 0.35 4
rs1876453
CR2
0.851 0.160 1 207454573 intron variant G/A snv 8.4E-02 4