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rs63750921

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750921(C;G)
Make rs63750921(G;G)
ReferenceGRCh38 38.1/141
Chromosome21
Position25891820
GeneAPP
is asnp
is mentioned by
dbSNPrs63750921
ebirs63750921
HLIrs63750921
Exacrs63750921
Varsomers63750921
Maprs63750921
PheGenIrs63750921
hapmaprs63750921
1000 genomesrs63750921
hgdprs63750921
ensemblrs63750921
gopubmedrs63750921
geneviewrs63750921
scholarrs63750921
googlers63750921
pharmgkbrs63750921
gwascentralrs63750921
openSNPrs63750921
23andMers63750921
23andMe allrs63750921
SNP Nexus

SNPshotrs63750921
SNPdbers63750921
MSV3drs63750921
GWAS Ctlgrs63750921
Max Magnitude0
OMIM104760
Desc
Variant0019
Relatedalso
ClinVar
Risk rs63750921(G;G)
Alt rs63750921(G;G)
Reference rs63750921(C;C)
Significance Pathogenic
Disease CEREBRAL AMYLOID ANGIOPATHY not provided
Variation info
Gene APP
CLNDBN CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, PIEDMONT VARIANT not provided
Reversed 1
HGVS NC_000021.8:g.27264132G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000019731.26, RCV000084565.1,