rs63750151

Orientation

minus

Stabilized

minus

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

Make rs63750151(C;C)

Reference

GRCh38.p7 38.3/150

Chromosome

21

Position

25891761

Gene

APP

is a	snp
is	mentioned by
dbSNP	rs63750151
dbSNP (classic)	rs63750151
ClinGen	rs63750151
ebi	rs63750151
HLI	rs63750151
Exac	rs63750151
Gnomad	rs63750151
Varsome	rs63750151
LitVar	rs63750151
Map	rs63750151
PheGenI	rs63750151
Biobank	rs63750151
1000 genomes	rs63750151
hgdp	rs63750151
ensembl	rs63750151
geneview	rs63750151
scholar	rs63750151
google	rs63750151
pharmgkb	rs63750151
gwascentral	rs63750151
openSNP	rs63750151
23andMe	rs63750151
SNPshot	rs63750151
SNPdbe	rs63750151
MSV3d	rs63750151
GWAS Ctlg	rs63750151

Max Magnitude

7

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,