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: rs13087058
rs13087058
1 3 73502077 intron variant T/C snv 0.26 0.700 1.000 1 2018 2018
dbSNP: rs4461368
rs4461368
1 3 73550154 intron variant C/T snv 0.72 0.700 1.000 1 2019 2019