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: rs284227
rs284227
1 1 81913762 intron variant C/T snv 0.77 0.700 1.000 1 2019 2019
dbSNP: rs651533
rs651533
1 1 81909877 intron variant T/A snv 0.78 0.700 1.000 1 2019 2019