Source: ALL
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: rs466448
rs466448
APP
4 0.925 0.040 21 26171790 intron variant A/C;G snv 0.010 1.000 1 2013 2013