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: rs1533269
rs1533269
1 3 114495764 intron variant C/A snv 0.43 0.700 1.000 1 2019 2019
dbSNP: rs2055981
rs2055981
1 3 114485122 intron variant T/C snv 0.49 0.700 1.000 1 2019 2019