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: rs3205166
rs3205166
DDX58
2 0.925 0.040 9 32459452 synonymous variant T/A;G snv 0.35 0.010 1.000 1 2011 2011
dbSNP: rs3804100
rs3804100
TLR2
36 0.633 0.720 4 153704257 synonymous variant T/C snv 9.0E-02 6.7E-02 0.010 1.000 1 2011 2011
dbSNP: rs4986790
rs4986790
TLR4
223 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1.000 1 2014 2014
dbSNP: rs5030710
rs5030710
TLR4
1 1.000 0.040 9 117712443 synonymous variant T/C snv 1.2E-02 4.7E-02 0.010 1.000 1 2011 2011
dbSNP: rs669260
rs669260
DDX58
4 0.851 0.080 9 32503442 intron variant T/A;C snv 0.010 1.000 1 2014 2014
dbSNP: rs763780
rs763780
IL17F
87 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 0.010 1.000 1 2014 2014