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: rs4958568
rs4958568
1 5 152636533 intron variant G/A snv 0.25 0.700 1.000 1 2018 2018
dbSNP: rs72799107
rs72799107
1 5 152673844 intron variant C/T snv 0.18 0.700 1.000 1 2018 2018