rs11162963

Orientation

plus

Stabilized

plus

Make rs11162963(C;C)

Make rs11162963(C;T)

Make rs11162963(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

80268896

is a	snp
is	mentioned by
dbSNP	rs11162963
dbSNP (classic)	rs11162963
ClinGen	rs11162963
ebi	rs11162963
HLI	rs11162963
Exac	rs11162963
Gnomad	rs11162963
Varsome	rs11162963
LitVar	rs11162963
Map	rs11162963
PheGenI	rs11162963
Biobank	rs11162963
1000 genomes	rs11162963
hgdp	rs11162963
ensembl	rs11162963
geneview	rs11162963
scholar	rs11162963
google	rs11162963
pharmgkb	rs11162963
gwascentral	rs11162963
openSNP	rs11162963
23andMe	rs11162963
SNPshot	rs11162963
SNPdbe	rs11162963
MSV3d	rs11162963
GWAS Ctlg	rs11162963

GMAF

0.4431

Max Magnitude

0

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

GWAS snp
PMID	[PMID 21782286]
Trait
Title	A genome-wide association study of aging.
Risk Allele	T
P-val	0.000004
Odds Ratio	1.0900 [NR]