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rs16827466

From SNPedia

Merged intors10494326
Orientationplus
Stabilizedplus
Make rs16827466(C;C)
Make rs16827466(C;T)
Make rs16827466(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position159679910
is asnp
is mentioned by
dbSNPrs16827466
ebirs16827466
HLIrs16827466
Exacrs16827466
Varsomers16827466
Maprs16827466
PheGenIrs16827466
hapmaprs16827466
1000 genomesrs16827466
hgdprs16827466
ensemblrs16827466
gopubmedrs16827466
geneviewrs16827466
scholarrs16827466
googlers16827466
pharmgkbrs16827466
gwascentralrs16827466
openSNPrs16827466
23andMers16827466
23andMe allrs16827466
SNP Nexus

SNPshotrs16827466
SNPdbers16827466
MSV3drs16827466
GWAS Ctlgrs16827466
StatusMerged into rs10494326
Max Magnitude
? (C;C) (C;T) (T;T) 28
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 T
P-val 4E-73
Odds Ratio .42 [0.37-0.46] unit increase