rs63751122

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;T)	7	Alzheimer's disease
(T;T)	0	common/normal

Make rs63751122(C;C)

Reference

GRCh38.p7 38.3/150

Chromosome

21

Position

25891765

Gene

APP

is a	snp
is	mentioned by
dbSNP	rs63751122
dbSNP (classic)	rs63751122
ClinGen	rs63751122
ebi	rs63751122
HLI	rs63751122
Exac	rs63751122
Gnomad	rs63751122
Varsome	rs63751122
LitVar	rs63751122
Map	rs63751122
PheGenI	rs63751122
Biobank	rs63751122
1000 genomes	rs63751122
hgdp	rs63751122
ensembl	rs63751122
geneview	rs63751122
scholar	rs63751122
google	rs63751122
pharmgkb	rs63751122
gwascentral	rs63751122
openSNP	rs63751122
23andMe	rs63751122
SNPshot	rs63751122
SNPdbe	rs63751122
MSV3d	rs63751122
GWAS Ctlg	rs63751122

Max Magnitude

7

aka Leu723Pro or L723P

AlzForum

ClinVar
Risk	rs63751122(C;C)
Alt	rs63751122(C;C)
Reference	Rs63751122(T;T)
Significance	Untested
Disease	not provided
Variation	info
Gene	APP
CLNDBN	not provided
Reversed	1
HGVS	NC_000021.8:g.27264077A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000084577.1,