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: rs11674595
rs11674595
IL1R2
13 0.763 0.200 2 101994530 intron variant T/C snv 0.22 0.010 1.000 1 2014 2014
dbSNP: rs1295686
rs1295686
IL13 ; TH2LCRR
7 0.882 0.160 5 132660151 intron variant T/A;C snv 0.68 0.010 1.000 1 2012 2012
dbSNP: rs2110726
rs2110726
IL1R1
2 2 102177822 3 prime UTR variant G/A snv 0.28 0.010 1.000 1 2012 2012