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: rs3820282
rs3820282
2 0.925 0.120 1 22141722 intron variant C/T snv 0.13 0.700 1.000 1 2015 2015
dbSNP: rs56318008
rs56318008
3 0.925 0.120 1 22143914 5 prime UTR variant C/T snv 0.13 0.010 1.000 1 2018 2018