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rs11763353

From SNPedia

Orientationplus
Stabilizedplus
Make rs11763353(A;A)
Make rs11763353(A;G)
Make rs11763353(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position15591246
is asnp
is mentioned by
dbSNPrs11763353
dbSNP (classic)rs11763353
ClinGenrs11763353
ebirs11763353
HLIrs11763353
Exacrs11763353
Gnomadrs11763353
Varsomers11763353
LitVarrs11763353
Maprs11763353
PheGenIrs11763353
Biobankrs11763353
1000 genomesrs11763353
hgdprs11763353
ensemblrs11763353
geneviewrs11763353
scholarrs11763353
googlers11763353
pharmgkbrs11763353
gwascentralrs11763353
openSNPrs11763353
23andMers11763353
SNPshotrs11763353
SNPdbers11763353
MSV3drs11763353
GWAS Ctlgrs11763353
GMAF0.1758
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 23720494OA-icon.png]
Trait Blood trace element (Zn levels)
Title Genome-wide association study identifies loci affecting blood copper, selenium and zinc.
Risk Allele
P-val 7E-7
Odds Ratio .19 [0.12-0.27] unit increase