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rs10931753

From SNPedia

Orientationplus
Stabilizedplus
Make rs10931753(C;C)
Make rs10931753(C;G)
Make rs10931753(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position153712244
is asnp
is mentioned by
dbSNPrs10931753
ebirs10931753
HLIrs10931753
Exacrs10931753
Varsomers10931753
Maprs10931753
PheGenIrs10931753
hapmaprs10931753
1000 genomesrs10931753
hgdprs10931753
ensemblrs10931753
gopubmedrs10931753
geneviewrs10931753
scholarrs10931753
googlers10931753
pharmgkbrs10931753
gwascentralrs10931753
openSNPrs10931753
23andMers10931753
23andMe allrs10931753
SNP Nexus

SNPshotrs10931753
SNPdbers10931753
MSV3drs10931753
GWAS Ctlgrs10931753
GMAF0.377
Max Magnitude
? (C;C) (C;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 5E-6
Odds Ratio .13 [0.074-0.184] unit increase