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rs4420065

From SNPedia

Orientationplus
Stabilizedplus
Make rs4420065(C;C)
Make rs4420065(C;T)
Make rs4420065(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position65695778
is asnp
is mentioned by
dbSNPrs4420065
ebirs4420065
HLIrs4420065
Exacrs4420065
Varsomers4420065
Maprs4420065
PheGenIrs4420065
hapmaprs4420065
1000 genomesrs4420065
hgdprs4420065
ensemblrs4420065
gopubmedrs4420065
geneviewrs4420065
scholarrs4420065
googlers4420065
pharmgkbrs4420065
gwascentralrs4420065
openSNPrs4420065
23andMers4420065
23andMe allrs4420065
SNP Nexus

SNPshotrs4420065
SNPdbers4420065
MSV3drs4420065
GWAS Ctlgrs4420065
GMAF0.4614
Max Magnitude
? (C;C) (C;T) (T;T) 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 C
P-val 4E-62
Odds Ratio 0.0900 [0.08-0.10] unit increase