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: rs10889677
rs10889677
40 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 0.010 1.000 1 2019 2019
dbSNP: rs2201841
rs2201841
14 0.716 0.440 1 67228519 intron variant A/G;T snv 0.010 1.000 1 2019 2019
dbSNP: rs2243248
rs2243248
IL4
9 0.763 0.240 5 132672952 upstream gene variant T/A;C;G snv 0.010 1.000 1 2019 2019
dbSNP: rs6908425
rs6908425
11 0.752 0.320 6 20728500 intron variant T/C snv 0.78 0.010 1.000 1 2017 2017
dbSNP: rs7517847
rs7517847
19 0.689 0.600 1 67215986 intron variant T/G snv 0.37 0.010 1.000 1 2019 2019