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rs12150338

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common on affy axiom data
Make rs12150338(C;T)
Make rs12150338(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position1730810
GeneWDR81
is asnp
is mentioned by
dbSNPrs12150338
ebirs12150338
HLIrs12150338
Exacrs12150338
Varsomers12150338
Maprs12150338
PheGenIrs12150338
hapmaprs12150338
1000 genomesrs12150338
hgdprs12150338
ensemblrs12150338
gopubmedrs12150338
geneviewrs12150338
scholarrs12150338
googlers12150338
pharmgkbrs12150338
gwascentralrs12150338
openSNPrs12150338
23andMers12150338
23andMe allrs12150338
SNP Nexus

SNPshotrs12150338
SNPdbers12150338
MSV3drs12150338
GWAS Ctlgrs12150338
GMAF0.0978
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20705733OA-icon.png]
Trait
Title Common Variants in the Calcium Sensing Receptor Gene are Associated with Total Serum Calcium Levels
Risk Allele T
P-val 7E-7
Odds Ratio 0.05 [NR] unit increase
GWAS snp
PMID [PMID 24068962OA-icon.png]
Trait Calcium levels
Title Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations.
Risk Allele T
P-val 2E-6
Odds Ratio .03 [0.018-0.042] unit increase


ClinVar
Risk rs12150338(T;T)
Alt rs12150338(T;T)
Reference rs12150338(C;C)
Significance Probable-non-pathogenic
Disease not specified
Variation info
Gene WDR81
CLNDBN not specified
Reversed 0
HGVS NC_000017.10:g.1634104C>T
CLNSRC ClinVar University of Chicago
CLNACC RCV000118854.2,