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: rs794726861
rs794726861
1 1.000 10 93600692 missense variant C/T snv 0.800 0
dbSNP: rs794726862
rs794726862
1 1.000 10 93600698 missense variant C/T snv 0.800 0