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rs2357266

From SNPedia

Orientationminus
Stabilizedminus
Make rs2357266(C;C)
Make rs2357266(C;T)
Make rs2357266(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position9784258
is asnp
is mentioned by
dbSNPrs2357266
ebirs2357266
HLIrs2357266
Exacrs2357266
Varsomers2357266
Maprs2357266
PheGenIrs2357266
hapmaprs2357266
1000 genomesrs2357266
hgdprs2357266
ensemblrs2357266
gopubmedrs2357266
geneviewrs2357266
scholarrs2357266
googlers2357266
pharmgkbrs2357266
gwascentralrs2357266
openSNPrs2357266
23andMers2357266
23andMe allrs2357266
SNP Nexus

SNPshotrs2357266
SNPdbers2357266
MSV3drs2357266
GWAS Ctlgrs2357266
GMAF0.3531
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20707712OA-icon.png]
Trait
Title A genome-wide association study of self-rated health
Risk Allele G
P-val 0.000004
Odds Ratio 0.02 [NR] unit decrease