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rs12582659

From SNPedia

Orientationplus
Stabilizedplus
Make rs12582659(C;C)
Make rs12582659(C;T)
Make rs12582659(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position75670748
is asnp
is mentioned by
dbSNPrs12582659
dbSNP (old)rs12582659
ClinGenrs12582659
ebirs12582659
HLIrs12582659
Exacrs12582659
Gnomadrs12582659
Varsomers12582659
Maprs12582659
PheGenIrs12582659
Biobankrs12582659
1000 genomesrs12582659
hgdprs12582659
ensemblrs12582659
gopubmedrs12582659
geneviewrs12582659
scholarrs12582659
googlers12582659
pharmgkbrs12582659
gwascentralrs12582659
openSNPrs12582659
23andMers12582659
23andMe allrs12582659
SNP Nexus

SNPshotrs12582659
SNPdbers12582659
MSV3drs12582659
GWAS Ctlgrs12582659
GMAF0.09871
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23720494OA-icon.png]
Trait Blood trace element (Cu levels)
Title Genome-wide association study identifies loci affecting blood copper, selenium and zinc.
Risk Allele
P-val 3E-6
Odds Ratio 1.26 [0.73-1.79] unit increase