rs4667682

Orientation

plus

Stabilized

plus

Make rs4667682(C;C)

Make rs4667682(C;T)

Make rs4667682(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

171271410

Gene	LOC105373737

is a	snp
is	mentioned by
dbSNP	rs4667682
dbSNP (classic)	rs4667682
ClinGen	rs4667682
ebi	rs4667682
HLI	rs4667682
Exac	rs4667682
Gnomad	rs4667682
Varsome	rs4667682
LitVar	rs4667682
Map	rs4667682
PheGenI	rs4667682
Biobank	rs4667682
1000 genomes	rs4667682
hgdp	rs4667682
ensembl	rs4667682
geneview	rs4667682
scholar	rs4667682
google	rs4667682
pharmgkb	rs4667682
gwascentral	rs4667682
openSNP	rs4667682
23andMe	rs4667682
SNPshot	rs4667682
SNPdbe	rs4667682
MSV3d	rs4667682
GWAS Ctlg	rs4667682

GMAF

0.225

Max Magnitude

0

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

GWAS snp
PMID	[PMID 22745009]
Trait
Title	Multiple loci influencing hippocampal degeneration identified by genome scan.
Risk Allele	C
P-val	0.000005
Odds Ratio	None None