Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35366573
CD46
0.882 0.120 1 207785101 missense variant C/T snv 1.5E-02 1.5E-02 3
rs10127939
FCGR3A
0.851 0.160 1 161548543 missense variant A/C;T snv 4.3E-02; 5.5E-02 5
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
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs3743930
MEFV
0.611 0.720 16 3254626 missense variant C/G;T snv 7.1E-02 43
rs1800897
PAX2
0.925 0.240 10 100809115 synonymous variant C/T snv 7.4E-02 0.13 2
rs2326369
MAVS
0.925 0.160 20 3862337 synonymous variant C/T snv 9.2E-02 0.11 2
rs1143679
ITGAM
0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 14
rs3819025
IL17A
0.752 0.480 6 52186476 intron variant G/A snv 0.13 8.5E-02 11
rs10847697
SLC15A4
0.882 0.200 12 128814840 synonymous variant G/A snv 0.13 9.1E-02 3
rs2230911
LOC105370032 ; P2RX7
0.807 0.360 12 121177328 missense variant C/G snv 0.14 0.12 6
rs1065489
CFH
0.695 0.440 1 196740644 missense variant G/T snv 0.20 0.15 19
rs800292
CFH
0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 33
rs12150220
NLRP1
0.724 0.360 17 5582047 missense variant A/T snv 0.37 0.33 14