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rs63750399

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs63750399(A;G)
Make rs63750399(G;G)
ReferenceGRCh38 38.1/141
Chromosome21
Position25891787
GeneAPP, LOC100288213
is asnp
is mentioned by
dbSNPrs63750399
ebirs63750399
HLIrs63750399
Exacrs63750399
Varsomers63750399
Maprs63750399
PheGenIrs63750399
hapmaprs63750399
1000 genomesrs63750399
hgdprs63750399
ensemblrs63750399
gopubmedrs63750399
geneviewrs63750399
scholarrs63750399
googlers63750399
pharmgkbrs63750399
gwascentralrs63750399
openSNPrs63750399
23andMers63750399
23andMe allrs63750399
SNP Nexus

SNPshotrs63750399
SNPdbers63750399
MSV3drs63750399
GWAS Ctlgrs63750399
Max Magnitude0
OMIM104760
Desc
Variant0011
Relatedalso


ClinVar
Risk rs63750399(G;G)
Alt rs63750399(G;G)
Reference rs63750399(A;A)
Significance Pathogenic
Disease Alzheimer disease not provided
Variation info
Gene APP
CLNDBN Alzheimer disease, type 1 not provided
Reversed 1
HGVS NC_000021.8:g.27264099T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000019723.27, RCV000084573.1,