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rs3847646

From SNPedia

Orientationplus
Stabilizedplus
Make rs3847646(C;C)
Make rs3847646(C;T)
Make rs3847646(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position2932493
is asnp
is mentioned by
dbSNPrs3847646
ebirs3847646
HLIrs3847646
Exacrs3847646
Varsomers3847646
Maprs3847646
PheGenIrs3847646
hapmaprs3847646
1000 genomesrs3847646
hgdprs3847646
ensemblrs3847646
gopubmedrs3847646
geneviewrs3847646
scholarrs3847646
googlers3847646
pharmgkbrs3847646
gwascentralrs3847646
openSNPrs3847646
23andMers3847646
23andMe allrs3847646
SNP Nexus

SNPshotrs3847646
SNPdbers3847646
MSV3drs3847646
GWAS Ctlgrs3847646
GMAF0.388
Max Magnitude
? (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 0.000005
Odds Ratio 0.03 [NR] unit decrease