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rs11232535

From SNPedia

Orientationplus
Stabilizedplus
Make rs11232535(C;C)
Make rs11232535(C;T)
Make rs11232535(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position81217766
is asnp
is mentioned by
dbSNPrs11232535
dbSNP (classic)rs11232535
ClinGenrs11232535
ebirs11232535
HLIrs11232535
Exacrs11232535
Gnomadrs11232535
Varsomers11232535
LitVarrs11232535
Maprs11232535
PheGenIrs11232535
Biobankrs11232535
1000 genomesrs11232535
hgdprs11232535
ensemblrs11232535
geneviewrs11232535
scholarrs11232535
googlers11232535
pharmgkbrs11232535
gwascentralrs11232535
openSNPrs11232535
23andMers11232535
SNPshotrs11232535
SNPdbers11232535
MSV3drs11232535
GWAS Ctlgrs11232535
GMAF0.1267
Max Magnitude0
? (C;C) (C;T) (T;T) 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 .33 [0.20-0.45] unit increase