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: rs1564855725
rs1564855725
5 0.882 0.160 11 6617621 splice region variant C/T snv 0.700 0
dbSNP: rs864309505
rs864309505
10 0.807 0.200 11 6615220 missense variant T/G snv 0.700 0