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rs12153606

From SNPedia

Orientationplus
Stabilizedplus
Make rs12153606(G;G)
Make rs12153606(G;T)
Make rs12153606(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position85287951
is asnp
is mentioned by
dbSNPrs12153606
ebirs12153606
HLIrs12153606
Exacrs12153606
Varsomers12153606
Maprs12153606
PheGenIrs12153606
hapmaprs12153606
1000 genomesrs12153606
hgdprs12153606
ensemblrs12153606
gopubmedrs12153606
geneviewrs12153606
scholarrs12153606
googlers12153606
pharmgkbrs12153606
gwascentralrs12153606
openSNPrs12153606
23andMers12153606
23andMe allrs12153606
SNP Nexus

SNPshotrs12153606
SNPdbers12153606
MSV3drs12153606
GWAS Ctlgrs12153606
GMAF0.09596
Max Magnitude
? (G;G) (G;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 2E-6
Odds Ratio .16 [0.092-0.226] unit increase