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: rs1457547311
rs1457547311
IL1RN
4 0.851 0.080 2 113131082 synonymous variant G/A snv 4.0E-06 0.010 < 0.001 1 2013 2013
dbSNP: rs4986791
rs4986791
TLR4
182 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 0.010 < 0.001 1 2013 2013
dbSNP: rs745738344
rs745738344
TNF
28 0.653 0.600 6 31576786 synonymous variant G/A snv 1.6E-05 1.4E-05 0.010 < 0.001 1 2013 2013
dbSNP: rs754342091
rs754342091
TLR4
7 0.790 0.200 9 117712421 missense variant A/G snv 3.2E-05 1.4E-05 0.010 < 0.001 1 2013 2013
dbSNP: rs780209935
rs780209935
CXCL8
1 1.000 0.040 4 73742000 stop gained G/A snv 8.0E-06 0.010 < 0.001 1 2013 2013