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: rs1028997
rs1028997
1 21 36159924 intron variant G/A snv 0.39 0.700 1.000 1 2018 2018
dbSNP: rs60409141
rs60409141
1 21 36141094 intron variant G/T snv 0.39 0.700 1.000 1 2018 2018