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: rs4251961
rs4251961
IL1RN
10 0.763 0.200 2 113116890 intron variant T/C snv 0.29 0.010 1.000 1 2014 2014
dbSNP: rs4308977
rs4308977
CR2
2 0.925 0.160 1 207473553 missense variant T/A;C snv 4.0E-06; 0.27 0.010 1.000 1 2018 2018
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 2015 2015
dbSNP: rs5743313
rs5743313
TLR3
4 0.851 0.200 4 186079213 intron variant C/T snv 0.19 0.010 1.000 1 2012 2012
dbSNP: rs587782477
rs587782477
APC
4 0.882 0.120 5 112775679 missense variant A/T snv 0.010 1.000 1 2001 2001
dbSNP: rs601338
rs601338
FUT2 ; LOC105447645
19 0.742 0.280 19 48703417 stop gained G/A snv 0.38 0.45 0.010 1.000 1 2019 2019
dbSNP: rs7309123
rs7309123
CLEC7A ; LOC105369655
8 0.807 0.280 12 10119994 intron variant G/C snv 0.42 0.010 1.000 1 2016 2016
dbSNP: rs868435969
rs868435969
VCP
3 0.925 0.280 9 35066710 missense variant G/A snv 0.010 1.000 1 2011 2011