Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs396991
FCGR3A
0.742 0.480 1 161544752 missense variant A/C;G;T snv 0.33; 4.1E-06 14
rs601162 0.925 0.160 9 29632144 upstream gene variant A/C;G;T snv 2
rs10127939
FCGR3A
0.851 0.160 1 161548543 missense variant A/C;T snv 4.3E-02; 5.5E-02 5
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs3746444
MIR499A ; MIR499B ; MYH7B ; LOC107985393
0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs6478109
TNFSF15
0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 12
rs172378
C1QA
0.790 0.240 1 22638945 synonymous variant A/G snv 0.49 0.51 11
rs4664308
LOC105373717 ; PLA2R1
0.851 0.160 2 160060986 intron variant A/G snv 0.30 4
rs2295415
CREM
0.882 0.160 10 35212510 3 prime UTR variant A/G snv 0.19 3
rs8012283
NIN
0.925 0.160 14 50767442 intron variant A/G snv 0.23 2
rs2157257
MYH9
1.000 0.160 22 36312293 intron variant A/G snv 0.52 1
rs28940579
MEFV
0.732 0.440 16 3243310 missense variant A/G;T snv 2.2E-03; 4.0E-06 13
rs2298804
FCER1A
0.851 0.240 1 159304102 missense variant A/G;T snv 6.6E-03 4
rs11057864
SCARB1
0.925 0.160 12 124851404 intron variant C/A snv 6.5E-02 2
rs274068
SLC5A11
0.925 0.160 16 24887651 intron variant C/A snv 0.74 2
rs352140
TLR9
0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 42
rs3824662
GATA3
0.752 0.320 10 8062245 intron variant C/A;T snv 11
rs114580964
PRRC2A
1.000 0.160 6 31636736 missense variant C/A;T snv 3.4E-03 1.4E-03 1
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs3743930
MEFV
0.611 0.720 16 3254626 missense variant C/G;T snv 7.1E-02 43
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs6897932
IL7R
0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 25
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs117026326
LOC101926943 ; GTF2I
0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 10
rs1456896 0.882 0.200 7 50264865 upstream gene variant C/T snv 0.67 5