{{Rsnum
|rsid=7935346
|Gene=C11orf49
|Chromosome=11
|position=46986828
|Orientation=plus
|GMAF=0.4679
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=C11orf49
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 4.7 | 37.4 | 57.9
| HCB | 37.0 | 47.4 | 15.6
| JPT | 50.9 | 38.2 | 10.9
| YRI | 60.1 | 35.7 | 4.2
| ASW | 30.4 | 60.7 | 8.9
| CHB | 37.0 | 47.4 | 15.6
| CHD | 46.3 | 41.7 | 12.0
| GIH | 6.1 | 40.8 | 53.1
| LWK | 44.0 | 48.6 | 7.3
| MEX | 0.0 | 0.0 | 0.0
| MKK | 19.4 | 51.6 | 29.0
| TSI | 2.0 | 36.4 | 61.6
| HapMapRevision=28
}}rs7935346 increases susceptibility to Osteoporotic fractures for carriers of the G allele {{PMID|18445777}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}