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rs10498760

From SNPedia

Orientationplus
Stabilizedplus
Make rs10498760(A;A)
Make rs10498760(A;C)
Make rs10498760(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position45396059
GeneRUNX2
is asnp
is mentioned by
dbSNPrs10498760
ebirs10498760
HLIrs10498760
Exacrs10498760
Varsomers10498760
Maprs10498760
PheGenIrs10498760
hapmaprs10498760
1000 genomesrs10498760
hgdprs10498760
ensemblrs10498760
gopubmedrs10498760
geneviewrs10498760
scholarrs10498760
googlers10498760
pharmgkbrs10498760
gwascentralrs10498760
openSNPrs10498760
23andMers10498760
23andMe allrs10498760
SNP Nexus

SNPshotrs10498760
SNPdbers10498760
MSV3drs10498760
GWAS Ctlgrs10498760
GMAF0.0629
Max Magnitude
? (A;A) (A;C) (C;C) 28
Rs10498760
PubMed [PMID 17878995]
Affy Probeset SNP_A-4211612
Affy Orientation reverse
On GW 5.0
Alleles A/B G/T
Ancestral A
Population Spain
Allele C
Case Freq.
Control Freq.
Odds Ratio Het
Odds Ratio Hom
Odds Ratio All -
Disease Bone mineral density, lower (BMD-L)


rs10498760 is in linkage disequilibrium with a polymorphism that increases susceptibility to Bone mineral density variations, lower for carriers of the C allele [PMID 17878995]


[PMID 17903294OA-icon.png] Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study.