rs9918508

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in complete genomics

Make rs9918508(C;T)

Make rs9918508(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

9499649

is a	snp
is	mentioned by
dbSNP	rs9918508
dbSNP (classic)	rs9918508
ClinGen	rs9918508
ebi	rs9918508
HLI	rs9918508
Exac	rs9918508
Gnomad	rs9918508
Varsome	rs9918508
LitVar	rs9918508
Map	rs9918508
PheGenI	rs9918508
Biobank	rs9918508
1000 genomes	rs9918508
hgdp	rs9918508
ensembl	rs9918508
geneview	rs9918508
scholar	rs9918508
google	rs9918508
pharmgkb	rs9918508
gwascentral	rs9918508
openSNP	rs9918508
23andMe	rs9918508
SNPshot	rs9918508
SNPdbe	rs9918508
MSV3d	rs9918508
GWAS Ctlg	rs9918508

GMAF

0.07025

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	0.000008
Odds Ratio	NR NR