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: rs142117234
rs142117234
IL4
1 1.000 0.080 5 132672844 upstream gene variant G/A snv 3.7E-03 0.700 1.000 1 2019 2019
dbSNP: rs2243250
rs2243250
IL4
61 0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 0.060 1.000 6 2012 2016
dbSNP: rs2070874
rs2070874
IL4
27 0.672 0.560 5 132674018 5 prime UTR variant C/T snv 0.28 0.28 0.050 1.000 5 2011 2016
dbSNP: rs2227284
rs2227284
IL4
12 0.732 0.480 5 132677033 intron variant T/C;G snv 0.030 1.000 3 2013 2015
dbSNP: rs79908535
rs79908535
3 0.882 0.280 5 132679856 missense variant G/A snv 6.8E-05 2.8E-05 0.020 1.000 2 2000 2008
dbSNP: rs1196477957
rs1196477957
1 1.000 0.080 5 132679782 missense variant G/A snv 4.0E-06 0.010 1.000 1 2007 2007
dbSNP: rs1329751852
rs1329751852
1 1.000 0.080 5 132679759 missense variant C/T snv 4.0E-06 7.0E-06 0.010 1.000 1 2011 2011
dbSNP: rs2243290
rs2243290
2 0.925 0.120 5 132682477 intron variant C/A snv 0.27 0.25 0.010 1.000 1 2013 2013
dbSNP: rs4986964
rs4986964
IL4
1 1.000 0.080 5 132674129 missense variant T/C snv 0.010 1.000 1 2004 2004