Rs10778213

Orientation

plus

is a	snp
is	mentioned by
dbSNP	rs10778213
PheGenI	rs10778213
nextbio	rs10778213
hapmap	rs10778213
1000 genomes	rs10778213
hgdp	rs10778213
ensembl	rs10778213
gopubmed	rs10778213
geneview	rs10778213
scholar	rs10778213
google	rs10778213
pharmgkb	rs10778213
gwascentral	rs10778213
openSNP	rs10778213
23andMe	rs10778213
23andMe all	rs10778213
SNP Nexus
SNPshot	rs10778213
SNPdbe	rs10778213
MSV3d	rs10778213

Chromosome

12

Orientation

plus

GMAF

0.3274

Position

103495151

Reference

GRCh37 37.1/131

Max Magnitude

Make rs10778213(C;C)

Make rs10778213(C;T)

Make rs10778213(T;T)

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

GWAS
SNP	rs10778213
PubMedID	[PMID 18439548]
Condition	C-reactive protein
Gene	Unknown
Risk Allele	G
pValue	1.00E-010
OR	0.12
95% CI	NR) mg/dl decreas

[PMID 18852197] Metabolic and cardiovascular traits: an abundance of recently identified common genetic variants.

[PMID 19060910] Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.

[PMID 19936222] Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.

[PMID 20031577] Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study.

[PMID 21647738] Genome-wide association with C-reactive protein levels in CLHNS: evidence for the CRP and HNF1A loci and their interaction with exposure to a pathogenic environment.

GET Evidence
rs10778213
aa_change
aa_change_short
impact	pathogenic
qualified_impact	Insufficiently evaluated pathogenic
overall_frequency	0.585938
summary