Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs2397084
IL17F
0.716 0.480 6 52237046 missense variant T/C snv 6.7E-02 6.1E-02 14
rs6897932
IL7R
0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 25
rs2004640
IRF5
0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26
rs1143679
ITGAM
0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 14
rs117026326
LOC101926943 ; GTF2I
0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 10
rs4664308
LOC105373717 ; PLA2R1
0.851 0.160 2 160060986 intron variant A/G snv 0.30 4
rs4984
LOC105374794 ; ADD2
0.925 0.160 2 70673271 synonymous variant G/A snv 0.12 0.15 3
rs958476
LOC107984410 ; BARX2
0.925 0.160 11 129451923 3 prime UTR variant T/A;G snv 2
rs7834765
LOC107986971
0.925 0.160 8 121263666 regulatory region variant G/T snv 0.32 2
rs1799964
LTA ; LOC100287329 ; TNF
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs61752717
MEFV
0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 72
rs3743930
MEFV
0.611 0.720 16 3254626 missense variant C/G;T snv 7.1E-02 43
rs28940579
MEFV
0.732 0.440 16 3243310 missense variant A/G;T snv 2.2E-03; 4.0E-06 13
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs3746444
MIR499A ; MIR499B ; MYH7B ; LOC107985393
0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs2157257
MYH9
1.000 0.160 22 36312293 intron variant A/G snv 0.52 1
rs8091180
NFATC1
1.000 0.160 18 79404243 intron variant G/A snv 0.46 3
rs8012283
NIN
0.925 0.160 14 50767442 intron variant A/G snv 0.23 2
rs11203368
PADI4
0.925 0.200 1 17340013 intron variant C/T snv 0.57 3
rs1635564
PADI4
0.925 0.160 1 17357031 intron variant T/A;G snv 2
rs6056923
PAK5
1.000 0.160 20 9840271 intron variant T/C snv 0.10 1
rs329498
PELI1
0.882 0.200 2 64100410 synonymous variant G/A;C;T snv 8.0E-06; 0.34 3
rs3792192
PLA2R1
0.925 0.160 2 160030364 intron variant G/A snv 0.35 2
rs11981433
PON2
0.882 0.240 7 95425028 intron variant T/C;G snv 4