rs11177669

Orientation

plus

Stabilized

plus

Make rs11177669(A;A)

Make rs11177669(A;G)

Make rs11177669(G;G)

Reference

GRCh38 38.1/141

Chromosome

12

Position

69434901

is a	snp
is	mentioned by
dbSNP	rs11177669
dbSNP (classic)	rs11177669
ClinGen	rs11177669
ebi	rs11177669
HLI	rs11177669
Exac	rs11177669
Gnomad	rs11177669
Varsome	rs11177669
LitVar	rs11177669
Map	rs11177669
PheGenI	rs11177669
Biobank	rs11177669
1000 genomes	rs11177669
hgdp	rs11177669
ensembl	rs11177669
geneview	rs11177669
scholar	rs11177669
google	rs11177669
pharmgkb	rs11177669
gwascentral	rs11177669
openSNP	rs11177669
23andMe	rs11177669
SNPshot	rs11177669
SNPdbe	rs11177669
MSV3d	rs11177669
GWAS Ctlg	rs11177669

GMAF

0.2938

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

GWAS snp
PMID	[PMID 18391951]
Trait	Height
Title	Many sequence variants affecting diversity of adult human height
Risk Allele	A
P-val	0.0000030000000000000001
Odds Ratio	4.50 [2.54-6.46] % SD taller