Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3212227
IL12B
0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 27
rs2234237
TREM1
0.763 0.280 6 41282728 missense variant T/A snv 0.13 0.12 9
rs1801197
CALCR
0.851 0.240 7 93426441 missense variant A/G snv 0.39 0.36 5
rs2232582
LBP
0.882 0.160 20 38350862 synonymous variant T/C snv 0.16 0.22 3
rs3775073
TLR1 ; TLR6
0.882 0.080 4 38828211 synonymous variant T/C snv 0.37 0.44 3
rs140189115
LBP
0.925 0.080 20 38360728 missense variant G/A snv 8.0E-06 7.0E-06 2