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: rs28939068
rs28939068
CST3
9 0.790 0.200 20 23635330 missense variant A/T snv 0.810 0.750 4 1989 2010
dbSNP: rs753737986
rs753737986
APP
2 0.925 0.200 21 26111983 missense variant T/A snv 4.0E-06 0.010 < 0.001 1 2007 2007