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rs10491003

From SNPedia

Orientationminus
Stabilizedminus
Make rs10491003(A;A)
Make rs10491003(A;G)
Make rs10491003(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position9286688
GeneLINC00709, LOC101928272
is asnp
is mentioned by
dbSNPrs10491003
dbSNP (classic)rs10491003
ClinGenrs10491003
ebirs10491003
HLIrs10491003
Exacrs10491003
Gnomadrs10491003
Varsomers10491003
LitVarrs10491003
Maprs10491003
PheGenIrs10491003
Biobankrs10491003
1000 genomesrs10491003
hgdprs10491003
ensemblrs10491003
geneviewrs10491003
scholarrs10491003
googlers10491003
pharmgkbrs10491003
gwascentralrs10491003
openSNPrs10491003
23andMers10491003
SNPshotrs10491003
SNPdbers10491003
MSV3drs10491003
GWAS Ctlgrs10491003
Max Magnitude0
? (A;A) (A;G) (G;G) 28


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 5E-9
Odds Ratio .03 [0.017-0.037] unit increase