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rs9958032

From SNPedia

Orientationplus
Stabilizedplus
Make rs9958032(C;C)
Make rs9958032(C;T)
Make rs9958032(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position41648346
is asnp
is mentioned by
dbSNPrs9958032
ebirs9958032
HLIrs9958032
Exacrs9958032
Varsomers9958032
Maprs9958032
PheGenIrs9958032
hapmaprs9958032
1000 genomesrs9958032
hgdprs9958032
ensemblrs9958032
gopubmedrs9958032
geneviewrs9958032
scholarrs9958032
googlers9958032
pharmgkbrs9958032
gwascentralrs9958032
openSNPrs9958032
23andMers9958032
23andMe allrs9958032
SNP Nexus

SNPshotrs9958032
SNPdbers9958032
MSV3drs9958032
GWAS Ctlgrs9958032
GMAF0.009642
Max Magnitude
? (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 3E-6
Odds Ratio 1.47 [0.85-2.08] unit increase