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: rs2227284
rs2227284
IL4
12 0.732 0.480 5 132677033 intron variant T/C;G snv 0.010 1.000 1 2017 2017
dbSNP: rs2243250
rs2243250
IL4
61 0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 0.010 1.000 1 2017 2017
dbSNP: rs2243267
rs2243267
IL4
3 0.882 0.160 5 132678194 intron variant G/A;C snv 0.010 1.000 1 2017 2017
dbSNP: rs2243270
rs2243270
IL4
2 0.925 0.120 5 132678417 intron variant A/G;T snv 0.010 1.000 1 2017 2017
dbSNP: rs2243289
rs2243289
3 0.882 0.240 5 132682440 intron variant A/G snv 0.26 0.23 0.010 1.000 1 2017 2017