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: rs1115535
rs1115535
1 20 48974027 intron variant T/C snv 0.18 0.700 1.000 1 2018 2018
dbSNP: rs6019535
rs6019535
1 20 48924980 intron variant G/A snv 0.37 0.700 1.000 1 2018 2018
dbSNP: rs6019537
rs6019537
1 20 48927067 intron variant G/A snv 0.62 0.700 1.000 1 2018 2018