Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs368234815
IFNL4
0.742 0.280 19 39248514 frameshift variant TT/G;T delins 15
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs1012068
DEPDC5
0.827 0.160 22 31869917 intron variant T/G snv 0.37 5
rs10776934 1.000 0.080 9 135137855 regulatory region variant T/G snv 0.74 1
rs1293762
OAS2
1.000 0.080 12 112993031 intron variant T/G snv 0.67 1
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs153109
IL27
0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs3747517
IFIH1
0.732 0.360 2 162272314 missense variant T/C snv 0.68 0.68 13
rs1126579
CXCR2
0.776 0.200 2 218136011 3 prime UTR variant T/C snv 0.62 8
rs5998152
DEPDC5
0.827 0.160 22 31867176 intron variant T/C snv 0.37 5
rs8103142
IFNL3
0.882 0.120 19 39244466 missense variant T/C snv 0.29 0.40 4
rs12989760
SH3YL1
0.925 0.120 2 250470 intron variant T/C snv 2
rs11966728 1.000 0.080 6 131955465 intron variant T/C snv 0.26 1
rs12980602 1.000 0.080 19 39262180 upstream gene variant T/C snv 0.25 1
rs6139030
ITPA
1.000 0.080 20 3207087 upstream gene variant T/C snv 8.6E-02 1
rs965469
C20orf194
1.000 0.080 20 3400902 intron variant T/C snv 0.20 1
rs641738
LOC112268246 ; TMC4 ; MBOAT7
0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs10814325
RECK
0.827 0.200 9 36036597 upstream gene variant T/A;C;G snv 7
rs2854117
APOC3
0.851 0.200 11 116829426 upstream gene variant T/A;C snv 6
rs2267716
CRHR2
0.851 0.120 7 30677027 intron variant T/A;C snv 4
rs1863918
ADAMTS2
0.882 0.160 5 179112381 3 prime UTR variant G/T snv 0.25 4
rs10877012
CYP27B1 ; METTL1
0.763 0.280 12 57768302 intron variant G/C;T snv 10
rs9695310
DDX58
0.851 0.120 9 32464137 intron variant G/C snv 0.52 4