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rs63750151

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;G) 7 Alzheimer's disease
(G;G) 0 common/normal


Make rs63750151(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome21
Position25891761
GeneAPP
is asnp
is mentioned by
dbSNPrs63750151
dbSNP (classic)rs63750151
ClinGenrs63750151
ebirs63750151
HLIrs63750151
Exacrs63750151
Gnomadrs63750151
Varsomers63750151
LitVarrs63750151
Maprs63750151
PheGenIrs63750151
Biobankrs63750151
1000 genomesrs63750151
hgdprs63750151
ensemblrs63750151
geneviewrs63750151
scholarrs63750151
googlers63750151
pharmgkbrs63750151
gwascentralrs63750151
openSNPrs63750151
23andMers63750151
23andMe allrs63750151
SNPshotrs63750151
SNPdbers63750151
MSV3drs63750151
GWAS Ctlgrs63750151
Max Magnitude7

aka Lys724Asn or K724N

AlzForum


ClinVar
Risk rs63750151(C;C)
Alt rs63750151(C;C)
Reference Rs63750151(G;G)
Significance Untested
Disease not provided
Variation info
Gene APP
CLNDBN not provided
Reversed 1
HGVS NC_000021.8:g.27264073C>G
CLNSRC
CLNACC RCV000084578.1,