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: rs1440372
rs1440372
1 15 66740813 non coding transcript exon variant T/C snv 0.78 0.700 1.000 3 2015 2019
dbSNP: rs2119260
rs2119260
1 15 66719608 intron variant T/A;C;G snv 0.700 1.000 1 2019 2019