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rs11066587

From SNPedia

Orientationplus
Stabilizedplus
Make rs11066587(C;C)
Make rs11066587(C;G)
Make rs11066587(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position113541851
is asnp
is mentioned by
dbSNPrs11066587
ebirs11066587
HLIrs11066587
Exacrs11066587
Varsomers11066587
Maprs11066587
PheGenIrs11066587
hapmaprs11066587
1000 genomesrs11066587
hgdprs11066587
ensemblrs11066587
gopubmedrs11066587
geneviewrs11066587
scholarrs11066587
googlers11066587
pharmgkbrs11066587
gwascentralrs11066587
openSNPrs11066587
23andMers11066587
23andMe allrs11066587
SNP Nexus

SNPshotrs11066587
SNPdbers11066587
MSV3drs11066587
GWAS Ctlgrs11066587
GMAF0.174
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 19197348OA-icon.png]
Trait Quantitative traits
Title Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae
Risk Allele G
P-val 0.000005
Odds Ratio 0.26 [NR] mg/L increase

C-reactive protein (CRP) levels being the quantitative trait associated with in [PMID 19197348OA-icon.png]


GET Evidence
rs11066587
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.164062
summary