{{Rsnum
|rsid=4548577
|Gene=C11orf49
|Chromosome=11
|position=46976961
|Orientation=plus
|GMAF=0.314
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=C11orf49
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 60.4 | 35.1 | 4.5
| HCB | 17.0 | 47.4 | 35.6
| JPT | 13.8 | 38.5 | 47.7
| YRI | 91.1 | 8.9 | 0.0
| ASW | 83.0 | 17.0 | 0.0
| CHB | 17.0 | 47.4 | 35.6
| CHD | 0.0 | 0.0 | 0.0
| GIH | 56.2 | 38.5 | 5.2
| LWK | 91.7 | 8.3 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 93.5 | 6.5 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{Report GE
|PubMed=18445777
|Source=journal
|AffyProbeset=SNP_A-2158992
|AffyOrientation=same
|AlleleA=C
|AlleleB=T
|onGW5=
|rsid=4548577
|ancestral=C
|RiskPopulation=Caucasian
|RiskAllele=C
|CaseFreq=
|ControlFreq=
|OddsRatioHet=
|OddsRatioHom=
|OddsRatioAll=1.08
|Disease=Osteoporotic fractures
|DiseaseSymbol=OP-F
}}

rs4548577 is in linkage disequilibrium with a polymorphism that increases susceptibility to Osteoporotic fractures 1.08 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 | HumanOmni1Quad}}