Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
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
rs352140
TLR9
0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 42
rs396991
FCGR3A
0.742 0.480 1 161544752 missense variant A/C;G;T snv 0.33; 4.1E-06 14
rs28940579
MEFV
0.732 0.440 16 3243310 missense variant A/G;T snv 2.2E-03; 4.0E-06 13
rs8193037
IL17A
0.752 0.320 6 52186311 upstream gene variant G/A;T snv 12
rs3824662
GATA3
0.752 0.320 10 8062245 intron variant C/A;T snv 11
rs10127939
FCGR3A
0.851 0.160 1 161548543 missense variant A/C;T snv 4.3E-02; 5.5E-02 5
rs11981433
PON2
0.882 0.240 7 95425028 intron variant T/C;G snv 4
rs2298804
FCER1A
0.851 0.240 1 159304102 missense variant A/G;T snv 6.6E-03 4
rs329498
PELI1
0.882 0.200 2 64100410 synonymous variant G/A;C;T snv 8.0E-06; 0.34 3
rs1635564
PADI4
0.925 0.160 1 17357031 intron variant T/A;G snv 2
rs601162 0.925 0.160 9 29632144 upstream gene variant A/C;G;T snv 2
rs6697139 0.925 0.160 1 161690906 intergenic variant G/A;T snv 2
rs7692514 0.925 0.160 4 65276878 intergenic variant G/A;C snv 2
rs958476
LOC107984410 ; BARX2
0.925 0.160 11 129451923 3 prime UTR variant T/A;G snv 2
rs114580964
PRRC2A
1.000 0.160 6 31636736 missense variant C/A;T snv 3.4E-03 1.4E-03 1
rs117026326
LOC101926943 ; GTF2I
0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 10
rs17008504 1.000 0.160 4 124718662 intergenic variant T/A snv 4.3E-02 1
rs5744168
TLR5
0.701 0.480 1 223111858 stop gained G/A snv 5.3E-02 4.4E-02 18
rs2397084
IL17F
0.716 0.480 6 52237046 missense variant T/C snv 6.7E-02 6.1E-02 14
rs11057864
SCARB1
0.925 0.160 12 124851404 intron variant C/A snv 6.5E-02 2
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs6056923
PAK5
1.000 0.160 20 9840271 intron variant T/C snv 0.10 1