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: rs17326656
rs17326656
1 2 48735152 intron variant G/T snv 0.21 0.700 1.000 3 2018 2019
dbSNP: rs4465809
rs4465809
1 2 48753368 intron variant G/T snv 0.39 0.700 1.000 1 2019 2019