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rs63750643

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs63750643(A;G)
Make rs63750643(G;G)
ReferenceGRCh38 38.1/141
Chromosome21
Position25891793
GeneAPP
is asnp
is mentioned by
dbSNPrs63750643
ebirs63750643
HLIrs63750643
Exacrs63750643
Varsomers63750643
Maprs63750643
PheGenIrs63750643
hapmaprs63750643
1000 genomesrs63750643
hgdprs63750643
ensemblrs63750643
gopubmedrs63750643
geneviewrs63750643
scholarrs63750643
googlers63750643
pharmgkbrs63750643
gwascentralrs63750643
openSNPrs63750643
23andMers63750643
23andMe allrs63750643
SNP Nexus

SNPshotrs63750643
SNPdbers63750643
MSV3drs63750643
GWAS Ctlgrs63750643
Max Magnitude0
OMIM104760
Desc
Variant0017
Relatedalso


ClinVar
Risk rs63750643(G;G)
Alt rs63750643(G;G)
Reference rs63750643(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.27264105T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000019730.27, RCV000084568.1,