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: rs200396597
rs200396597
APP
1.000 0.080 21 25881743 missense variant C/T snv 7.0E-06
CUI: C0036572
Disease: Seizures
Seizures 		0.010 1.000 1 2018 2018
dbSNP: rs200396597
rs200396597
APP
1.000 0.080 21 25881743 missense variant C/T snv 7.0E-06
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.010 < 0.001 1 2018 2018