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rs494562

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs494562(C;C)
Make rs494562(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position85407411
is asnp
is mentioned by
dbSNPrs494562
ebirs494562
HLIrs494562
Exacrs494562
Varsomers494562
Maprs494562
PheGenIrs494562
hapmaprs494562
1000 genomesrs494562
hgdprs494562
ensemblrs494562
gopubmedrs494562
geneviewrs494562
scholarrs494562
googlers494562
pharmgkbrs494562
gwascentralrs494562
openSNPrs494562
23andMers494562
23andMe allrs494562
SNP Nexus

SNPshotrs494562
SNPdbers494562
MSV3drs494562
GWAS Ctlgrs494562
GMAF0.1529
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21886157OA-icon.png]
Trait
Title Human metabolic individuality in biomedical and pharmaceutical research.
Risk Allele G
P-val 7E-13
Odds Ratio 0.3020 None
GWAS snp
PMID [PMID 24816252OA-icon.png]
Trait Blood metabolite levels
Title An atlas of genetic influences on human blood metabolites.
Risk Allele A
P-val 1E-12
Odds Ratio .12 [0.085-0.151] unit decrease