rs10867752

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common on affy axiom data

Make rs10867752(C;T)

Make rs10867752(T;T)

Reference

GRCh38 38.1/141

Chromosome

9

Position

81400122

is a	snp
is	mentioned by
dbSNP	rs10867752
dbSNP (classic)	rs10867752
ClinGen	rs10867752
ebi	rs10867752
HLI	rs10867752
Exac	rs10867752
Gnomad	rs10867752
Varsome	rs10867752
LitVar	rs10867752
Map	rs10867752
PheGenI	rs10867752
Biobank	rs10867752
1000 genomes	rs10867752
hgdp	rs10867752
ensembl	rs10867752
geneview	rs10867752
scholar	rs10867752
google	rs10867752
pharmgkb	rs10867752
gwascentral	rs10867752
openSNP	rs10867752
23andMe	rs10867752
SNPshot	rs10867752
SNPdbe	rs10867752
MSV3d	rs10867752
GWAS Ctlg	rs10867752

GMAF

0.08815

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

GWAS snp
PMID	[PMID 19668339]
Trait	Hippocampal atrophy
Title	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease
Risk Allele
P-val	0.000003
Odds Ratio	NR NR