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rs6752877

From SNPedia

Orientationplus
Stabilizedplus
Make rs6752877(G;G)
Make rs6752877(G;T)
Make rs6752877(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position54434432
GeneLOC102724072
is asnp
is mentioned by
dbSNPrs6752877
ebirs6752877
HLIrs6752877
Exacrs6752877
Varsomers6752877
Maprs6752877
PheGenIrs6752877
hapmaprs6752877
1000 genomesrs6752877
hgdprs6752877
ensemblrs6752877
gopubmedrs6752877
geneviewrs6752877
scholarrs6752877
googlers6752877
pharmgkbrs6752877
gwascentralrs6752877
openSNPrs6752877
23andMers6752877
23andMe allrs6752877
SNP Nexus

SNPshotrs6752877
SNPdbers6752877
MSV3drs6752877
GWAS Ctlgrs6752877
GMAF0.1763
Max Magnitude
? (G;G) (G;T) (T;T) 28
Rs6752877
PubMed [PMID 18445777]
Affy Probeset SNP_A-2263153
Affy Orientation reverse
On GW 5.0
Alleles A/B A/C
Ancestral T
Population Caucasian
Allele T
Case Freq.
Control Freq.
Odds Ratio Het
Odds Ratio Hom
Odds Ratio All 1.11
Disease Osteoporotic fractures (OP-F)


rs6752877 is in linkage disequilibrium with a polymorphism that increases susceptibility to Osteoporotic fractures 1.11 times for carriers of the T allele [PMID 18445777]