Rs10778213

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ReferenceGRCh38 38.1/141
Chromosome12
Position103101373
is asnp
is mentioned by
dbSNPrs10778213
Exacrs10778213
PheGenIrs10778213
nextbiors10778213
hapmaprs10778213
1000 genomesrs10778213
hgdprs10778213
ensemblrs10778213
gopubmedrs10778213
geneviewrs10778213
scholarrs10778213
googlers10778213
pharmgkbrs10778213
gwascentralrs10778213
openSNPrs10778213
23andMers10778213
23andMe allrs10778213
SNP Nexus

SNPshotrs10778213
SNPdbers10778213
MSV3drs10778213
GMAF0.3274
? (C;C) (C;T) (T;T) 28
GWAS
SNP rs10778213
PubMedID [PMID 18439548OA-icon.png]
Condition C-reactive protein
Gene Unknown
Risk Allele G
pValue 1.00E-010
OR 0.12
95% CI NR) mg/dl decreas




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


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


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


[PMID 20031577OA-icon.png] 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 21647738OA-icon.png] 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