{{Rsnum
|rsid=6426748
|Chromosome=1
|position=22381072
|Orientation=plus
|GMAF=0.185
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 71.7 | 27.4 | 0.9
| HCB | 56.2 | 40.1 | 3.6
| JPT | 61.1 | 36.3 | 2.7
| YRI | 42.9 | 48.3 | 8.8
| ASW | 63.2 | 33.3 | 3.5
| CHB | 56.2 | 40.1 | 3.6
| CHD | 65.1 | 30.3 | 4.6
| GIH | 79.2 | 18.8 | 2.0
| LWK | 51.8 | 38.2 | 10.0
| MEX | 91.4 | 8.6 | 0.0
| MKK | 48.7 | 42.9 | 8.3
| TSI | 80.4 | 18.6 | 1.0
| HapMapRevision=28
}}{{Report GE
|PubMed=18445777
|Source=journal
|AffyProbeset=SNP_A-2276784
|AffyOrientation=same
|AlleleA=C
|AlleleB=T
|onGW5=
|rsid=6426748
|ancestral=C
|RiskPopulation=Caucasian
|RiskAllele=C
|CaseFreq=
|ControlFreq=
|OddsRatioHet=
|OddsRatioHom=
|OddsRatioAll=-
|Disease=Bone mineral density, lower
|DiseaseSymbol=BMD-L
}}

rs6426748 is in linkage disequilibrium with a polymorphism that increases susceptibility to Bone mineral density variations, lower for carriers of the C allele {{PMID|18445777}}

rs6426748 is in linkage disequilibrium with a polymorphism that increases susceptibility to Osteoporotic fractures 1.15 times for carriers of the C 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}}