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rs9831754

From SNPedia

Orientationplus
Stabilizedplus
Make rs9831754(G;G)
Make rs9831754(G;T)
Make rs9831754(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position78304441
is asnp
is mentioned by
dbSNPrs9831754
ebirs9831754
HLIrs9831754
Exacrs9831754
Varsomers9831754
Maprs9831754
PheGenIrs9831754
hapmaprs9831754
1000 genomesrs9831754
hgdprs9831754
ensemblrs9831754
gopubmedrs9831754
geneviewrs9831754
scholarrs9831754
googlers9831754
pharmgkbrs9831754
gwascentralrs9831754
openSNPrs9831754
23andMers9831754
23andMe allrs9831754
SNP Nexus

SNPshotrs9831754
SNPdbers9831754
MSV3drs9831754
GWAS Ctlgrs9831754
GMAF0.2557
Max Magnitude
? (G;G) (G;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 0.000008
Odds Ratio 0.02 [NR] unit decrease