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rs63750363

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750363(C;C)
Make rs63750363(C;G)
ReferenceGRCh38 38.1/141
Chromosome21
Position25897642
GeneAPP
is asnp
is mentioned by
dbSNPrs63750363
ebirs63750363
HLIrs63750363
Exacrs63750363
Varsomers63750363
Maprs63750363
PheGenIrs63750363
hapmaprs63750363
1000 genomesrs63750363
hgdprs63750363
ensemblrs63750363
gopubmedrs63750363
geneviewrs63750363
scholarrs63750363
googlers63750363
pharmgkbrs63750363
gwascentralrs63750363
openSNPrs63750363
23andMers63750363
23andMe allrs63750363
SNP Nexus

SNPshotrs63750363
SNPdbers63750363
MSV3drs63750363
GWAS Ctlgrs63750363
Max Magnitude0
OMIM104760
Desc
Variant0010
Relatedalso


ClinVar
Risk rs63750363(C;C)
Alt rs63750363(C;C)
Reference rs63750363(G;G)
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.27269954C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000019722.27, RCV000084557.1,