rs10521222

Orientation

plus

Stabilized

plus

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

Make rs10521222(C;T)

Make rs10521222(T;T)

Reference

GRCh38 38.1/141

Chromosome

16

Position

51124799

is a	snp
is	mentioned by
dbSNP	rs10521222
dbSNP (classic)	rs10521222
ClinGen	rs10521222
ebi	rs10521222
HLI	rs10521222
Exac	rs10521222
Gnomad	rs10521222
Varsome	rs10521222
LitVar	rs10521222
Map	rs10521222
PheGenI	rs10521222
Biobank	rs10521222
1000 genomes	rs10521222
hgdp	rs10521222
ensembl	rs10521222
geneview	rs10521222
scholar	rs10521222
google	rs10521222
pharmgkb	rs10521222
gwascentral	rs10521222
openSNP	rs10521222
23andMe	rs10521222
SNPshot	rs10521222
SNPdbe	rs10521222
MSV3d	rs10521222
GWAS Ctlg	rs10521222

GMAF

0.02342

Max Magnitude

0

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

GWAS snp
PMID	[PMID 21300955]
Trait
Title	Meta-Analysis of Genome-Wide Association Studies in >80 000 Subjects Identifies Multiple Loci for C-Reactive Protein Levels
Risk Allele	C
P-val	9E-13
Odds Ratio	0.1040 [0.07-0.13] unit increase