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rs63750734

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750734(A;A)
Make rs63750734(A;G)
ReferenceGRCh38 38.1/141
Chromosome21
Position25891790
GeneAPP
is asnp
is mentioned by
dbSNPrs63750734
ebirs63750734
HLIrs63750734
Exacrs63750734
Varsomers63750734
Maprs63750734
PheGenIrs63750734
hapmaprs63750734
1000 genomesrs63750734
hgdprs63750734
ensemblrs63750734
gopubmedrs63750734
geneviewrs63750734
scholarrs63750734
googlers63750734
pharmgkbrs63750734
gwascentralrs63750734
openSNPrs63750734
23andMers63750734
23andMe allrs63750734
SNP Nexus

SNPshotrs63750734
SNPdbers63750734
MSV3drs63750734
GWAS Ctlgrs63750734
Max Magnitude0
OMIM104760
Desc
Variant0012
Relatedalso


ClinVar
Risk rs63750734(A;A)
Alt rs63750734(A;A)
Reference rs63750734(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.27264102C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019724.27, RCV000084570.1,