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rs6734238

From SNPedia

Orientationplus
Stabilizedplus
Make rs6734238(A;A)
Make rs6734238(A;G)
Make rs6734238(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position113083453
is asnp
is mentioned by
dbSNPrs6734238
ebirs6734238
HLIrs6734238
Exacrs6734238
Varsomers6734238
Maprs6734238
PheGenIrs6734238
hapmaprs6734238
1000 genomesrs6734238
hgdprs6734238
ensemblrs6734238
gopubmedrs6734238
geneviewrs6734238
scholarrs6734238
googlers6734238
pharmgkbrs6734238
gwascentralrs6734238
openSNPrs6734238
23andMers6734238
23andMe allrs6734238
SNP Nexus

SNPshotrs6734238
SNPdbers6734238
MSV3drs6734238
GWAS Ctlgrs6734238
GMAF0.3163
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21300955OA-icon.png]
Trait
Title Meta-Analysis of Genome-Wide Association Studies in >80 000 Subjects Identifies Multiple Loci for C-Reactive Protein Levels
Risk Allele G
P-val 2E-17
Odds Ratio 0.0500 [0.04-0.06] unit increase
GWAS snp
PMID [PMID 22939635OA-icon.png]
Trait C-reactive protein
Title Genome-wide association and population genetic analysis of C-reactive protein in African American and Hispanic American women.
Risk Allele G
P-val 9E-10
Odds Ratio .11 [0.073-0.143] unit decrease
GWAS snp
PMID [PMID 23969696OA-icon.png]
Trait Fibrinogen
Title Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease.
Risk Allele A
P-val 6E-19
Odds Ratio .01 [0.007-0.011] unit decrease