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: rs2070874
rs2070874
IL4
27 0.672 0.560 5 132674018 5 prime UTR variant C/T snv 0.28 0.28 0.010 1.000 1 2019 2019
dbSNP: rs2355767
rs2355767 		1 1.000 0.080 7 11921939 intergenic variant G/A;C;T snv 0.010 1.000 1 2019 2019
dbSNP: rs3796704
rs3796704
ENAM
3 0.882 0.120 4 70643714 missense variant G/A snv 7.0E-02 0.13 0.010 1.000 1 2013 2013
dbSNP: rs7526319
rs7526319
TUFT1
1 1.000 0.080 1 151552082 intron variant T/C snv 0.54 0.010 1.000 1 2019 2019