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: rs1191926239
rs1191926239
TLR4
7 0.807 0.200 9 117704539 missense variant C/G snv 4.0E-06 0.010 1.000 1 2004 2004
dbSNP: rs1800450
rs1800450
MBL2
26 0.662 0.640 10 52771475 missense variant C/T snv 0.14 0.11 0.010 1.000 1 2017 2017
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 2004 2004
dbSNP: rs754342091
rs754342091
TLR4
7 0.790 0.200 9 117712421 missense variant A/G snv 3.2E-05 1.4E-05 0.010 1.000 1 2004 2004