Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs950592627
rs950592627
APP
0.827 0.200 21 26090015 missense variant G/C snv 7.0E-06
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.020 1.000 2 2001 2008
dbSNP: rs950592627
rs950592627
APP
0.827 0.200 21 26090015 missense variant G/C snv 7.0E-06
CUI: C0085220
Disease: Cerebral Amyloid Angiopathy
Cerebral Amyloid Angiopathy 		0.010 1.000 1 2005 2005
dbSNP: rs950592627
rs950592627
APP
0.827 0.200 21 26090015 missense variant G/C snv 7.0E-06
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		0.010 1.000 1 2001 2001
dbSNP: rs950592627
rs950592627
APP
0.827 0.200 21 26090015 missense variant G/C snv 7.0E-06
CUI: C0740340
Disease: Amyloidosis, Familial
Amyloidosis, Familial 		0.010 1.000 1 1994 1994
dbSNP: rs950592627
rs950592627
APP
0.827 0.200 21 26090015 missense variant G/C snv 7.0E-06
CUI: C0002726
Disease: Amyloidosis
Amyloidosis 		0.010 1.000 1 2011 2011