Gene: APP ×
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: rs371425292
rs371425292
APP
10 0.763 0.160 21 25897627 missense variant C/A;T snv 8.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs529782627
rs529782627
APP
3 0.882 0.120 21 26112051 missense variant C/A snv 4.0E-06 7.0E-06 0.010 1.000 1 2012 2012
dbSNP: rs572842823
rs572842823
APP
11 0.763 0.160 21 25897626 missense variant T/A;G snv 0.010 1.000 1 2010 2010
dbSNP: rs63750847
rs63750847
APP
8 0.790 0.120 21 25897620 missense variant C/T snv 4.5E-04 3.0E-04 0.010 1.000 1 2017 2017
dbSNP: rs63751039
rs63751039
APP
8 0.776 0.200 21 25891855 missense variant T/C snv 0.010 1.000 1 2013 2013
dbSNP: rs763852444
rs763852444
APP
3 0.882 0.120 21 26112127 missense variant G/C snv 4.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs781049584
rs781049584
APP
18 0.724 0.280 21 26021917 missense variant T/G snv 8.2E-06 7.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs950592627
rs950592627
APP
5 0.827 0.200 21 26090015 missense variant G/C snv 7.0E-06 0.010 1.000 1 2011 2011