{{Rsnum
|rsid=2957137
|Chromosome=18
|position=62399655
|Orientation=plus
|GMAF=0.4316
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 8.8 | 50.4 | 40.7
| HCB | 48.2 | 40.1 | 11.7
| JPT | 46.0 | 39.8 | 14.2
| YRI | 6.8 | 41.5 | 51.7
| ASW | 5.3 | 33.3 | 61.4
| CHB | 48.2 | 40.1 | 11.7
| CHD | 40.4 | 50.5 | 9.2
| GIH | 15.8 | 44.6 | 39.6
| LWK | 6.4 | 41.8 | 51.8
| MEX | 6.9 | 58.6 | 34.5
| MKK | 5.1 | 41.0 | 53.8
| TSI | 7.8 | 48.0 | 44.1
| HapMapRevision=28
}}

{{Report GE
|PubMed=18445777
|Source=journal
|AffyProbeset=SNP_A-8507078
|AffyOrientation=reverse
|AlleleA=A
|AlleleB=T
|onGW5=
|rsid=2957137
|ancestral=T
|RiskPopulation=Caucasian
|RiskAllele=A
|CaseFreq=
|ControlFreq=
|OddsRatioHet=
|OddsRatioHom=
|OddsRatioAll=1.08
|Disease=Osteoporotic fractures
|DiseaseSymbol=OP-F
}}

rs2957137 is in linkage disequilibrium with a polymorphism that increases susceptibility to Osteoporotic fractures 1.08 times for carriers of the A allele {{PMID|18445777}}

{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}