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rs63749964

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;T) 7 Maybe: Alzheimer's disease; possible miscall for 23andMe users though
(T;T) 0 common in clinvar


Make rs63749964(G;G)
ReferenceGRCh38 38.1/141
Chromosome21
Position25891783
GeneAPP
is asnp
is mentioned by
dbSNPrs63749964
dbSNP (old)rs63749964
ClinGenrs63749964
ebirs63749964
HLIrs63749964
Exacrs63749964
Gnomadrs63749964
Varsomers63749964
Maprs63749964
PheGenIrs63749964
Biobankrs63749964
1000 genomesrs63749964
hgdprs63749964
ensemblrs63749964
gopubmedrs63749964
geneviewrs63749964
scholarrs63749964
googlers63749964
pharmgkbrs63749964
gwascentralrs63749964
openSNPrs63749964
23andMers63749964
23andMe allrs63749964
SNP Nexus

SNPshotrs63749964
SNPdbers63749964
MSV3drs63749964
GWAS Ctlgrs63749964
Max Magnitude7

c.2150T>G, p.Val717Gly, V717G

AlzForum

OMIM104760
Desc
Variant0004
Relatedalso


ClinVar
Risk rs63749964(G;G)
Alt rs63749964(G;G)
Reference Rs63749964(T;T)
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.27264095A>C
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000019716.27, RCV000084576.1,