rs16867321

Orientation

plus

Stabilized

plus

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

Make rs16867321(C;T)

Make rs16867321(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

180497652

is a	snp
is	mentioned by
dbSNP	rs16867321
dbSNP (classic)	rs16867321
ClinGen	rs16867321
ebi	rs16867321
HLI	rs16867321
Exac	rs16867321
Gnomad	rs16867321
Varsome	rs16867321
LitVar	rs16867321
Map	rs16867321
PheGenI	rs16867321
Biobank	rs16867321
1000 genomes	rs16867321
hgdp	rs16867321
ensembl	rs16867321
geneview	rs16867321
scholar	rs16867321
google	rs16867321
pharmgkb	rs16867321
gwascentral	rs16867321
openSNP	rs16867321
23andMe	rs16867321
SNPshot	rs16867321
SNPdbe	rs16867321
MSV3d	rs16867321
GWAS Ctlg	rs16867321

GMAF

0.2713

Max Magnitude

0

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

GWAS snp
PMID	[PMID 21552555]
Trait
Title	A genome-wide association study on obesity and obesity-related traits.
Risk Allele
P-val	0.000002
Odds Ratio	None None