{{Rsnum
|rsid=6752877
|Chromosome=2
|position=54434432
|Orientation=plus
|GMAF=0.1763
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=LOC102724072
|Gene_s=LOC102724072
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 15.0 | 48.7 | 36.3
| HCB | 0.0 | 5.8 | 94.2
| JPT | 0.0 | 2.7 | 97.3
| YRI | 0.0 | 6.8 | 93.2
| ASW | 0.0 | 14.0 | 86.0
| CHB | 0.0 | 5.8 | 94.2
| CHD | 0.0 | 12.8 | 87.2
| GIH | 2.0 | 31.7 | 66.3
| LWK | 0.0 | 7.3 | 92.7
| MEX | 3.4 | 27.6 | 69.0
| MKK | 0.0 | 7.1 | 92.9
| TSI | 6.9 | 51.0 | 42.2
| HapMapRevision=28
}}{{Report GE
|PubMed=18445777
|Source=journal
|AffyProbeset=SNP_A-2263153
|AffyOrientation=reverse
|AlleleA=A
|AlleleB=C
|onGW5=
|rsid=6752877
|ancestral=T
|RiskPopulation=Caucasian
|RiskAllele=T
|CaseFreq=
|ControlFreq=
|OddsRatioHet=
|OddsRatioHom=
|OddsRatioAll=1.11
|Disease=Osteoporotic fractures
|DiseaseSymbol=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}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Affy500k}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}