rs63750363

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs63750363(C;C)

Make rs63750363(C;G)

Reference

GRCh38 38.1/141

Chromosome

21

Position

25897642

Gene

APP

is a	snp
is	mentioned by
dbSNP	rs63750363
dbSNP (classic)	rs63750363
ClinGen	rs63750363
ebi	rs63750363
HLI	rs63750363
Exac	rs63750363
Gnomad	rs63750363
Varsome	rs63750363
LitVar	rs63750363
Map	rs63750363
PheGenI	rs63750363
Biobank	rs63750363
1000 genomes	rs63750363
hgdp	rs63750363
ensembl	rs63750363
geneview	rs63750363
scholar	rs63750363
google	rs63750363
pharmgkb	rs63750363
gwascentral	rs63750363
openSNP	rs63750363
23andMe	rs63750363
SNPshot	rs63750363
SNPdbe	rs63750363
MSV3d	rs63750363
GWAS Ctlg	rs63750363

Max Magnitude

0

OMIM	104760
Desc
Variant	0010
Related	also

ClinVar
Risk	rs63750363(C;C)
Alt	rs63750363(C;C)
Reference	Rs63750363(G;G)
Significance	Pathogenic
Disease	Alzheimer disease not provided not specified
Variation	info
Gene	APP
CLNDBN	Alzheimer disease, type 1 not provided not specified
Reversed	1
HGVS	NC_000021.8:g.27269954C>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000019722.27, RCV000084557.1, RCV000480114.1,