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: rs79020217
rs79020217
1 1.000 0.120 6 29672739 missense variant G/C snv 0.800 1.000 1 2000 2000