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rs6091737

From SNPedia

Orientationplus
Stabilizedplus
Make rs6091737(C;C)
Make rs6091737(C;T)
Make rs6091737(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position53733353
is asnp
is mentioned by
dbSNPrs6091737
ebirs6091737
HLIrs6091737
Exacrs6091737
Varsomers6091737
Maprs6091737
PheGenIrs6091737
hapmaprs6091737
1000 genomesrs6091737
hgdprs6091737
ensemblrs6091737
gopubmedrs6091737
geneviewrs6091737
scholarrs6091737
googlers6091737
pharmgkbrs6091737
gwascentralrs6091737
openSNPrs6091737
23andMers6091737
23andMe allrs6091737
SNP Nexus

SNPshotrs6091737
SNPdbers6091737
MSV3drs6091737
GWAS Ctlgrs6091737
GMAF0.2971
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 0.000006
Odds Ratio 0.02 [NR] unit decrease