Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1143634
rs1143634
IL1B
52 0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 0.020 1.000 2 2014 2017
dbSNP: rs1130864
rs1130864
CRP
27 0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 0.010 1.000 1 2017 2017
dbSNP: rs1205
rs1205
CRP
46 0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 0.010 1.000 1 2017 2017
dbSNP: rs140189115
rs140189115
LBP
2 0.925 0.080 20 38360728 missense variant G/A snv 8.0E-06 7.0E-06 0.010 1.000 1 2009 2009
dbSNP: rs1801197
rs1801197
CALCR
5 0.851 0.240 7 93426441 missense variant A/G snv 0.39 0.36 0.010 1.000 1 2017 2017
dbSNP: rs2232582
rs2232582
LBP
3 0.882 0.160 20 38350862 synonymous variant T/C snv 0.16 0.22 0.010 1.000 1 2009 2009
dbSNP: rs2234237
rs2234237
TREM1
9 0.763 0.280 6 41282728 missense variant T/A snv 0.13 0.12 0.010 1.000 1 2015 2015
dbSNP: rs3212227
rs3212227
IL12B
65 0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 0.010 1.000 1 2017 2017
dbSNP: rs3775073
rs3775073
TLR1 ; TLR6
3 0.882 0.080 4 38828211 synonymous variant T/C snv 0.37 0.44 0.010 < 0.001 1 2015 2015