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rs11084337

From SNPedia

Orientationplus
Stabilizedplus
Make rs11084337(C;C)
Make rs11084337(C;T)
Make rs11084337(T;T)
ReferenceGRCh37.p10 37.5/138
Chromosome19
Position54916104
is asnp
is mentioned by
dbSNPrs11084337
ebirs11084337
HLIrs11084337
Exacrs11084337
Varsomers11084337
Maprs11084337
PheGenIrs11084337
hapmaprs11084337
1000 genomesrs11084337
hgdprs11084337
ensemblrs11084337
gopubmedrs11084337
geneviewrs11084337
scholarrs11084337
googlers11084337
pharmgkbrs11084337
gwascentralrs11084337
openSNPrs11084337
23andMers11084337
23andMe allrs11084337
SNP Nexus

SNPshotrs11084337
SNPdbers11084337
MSV3drs11084337
GWAS Ctlgrs11084337
GMAF0.4821
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23720494OA-icon.png]
Trait Blood trace element (Se levels)
Title Genome-wide association study identifies loci affecting blood copper, selenium and zinc.
Risk Allele
P-val 9E-7
Odds Ratio .13 [0.081-0.187] unit increase