{{Rsnum
|rsid = 28934587
|Gene = BBS1
|geno1 = (C;C)
|geno2 = (C;T)
|geno3 = (T;T)
|Orientation=plus
|ReferenceAllele=T
|MissenseAllele=C
|Chromosome=11
|position=66299182
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
|Status=Deleted
}}{{omim
| id = 209901
| variant = 0005
| desc    = BARDET-BIEDL SYNDROME 1
| rsnum   = 28934587
}}

[[Bardet-Biedl syndrome]] is a genetic disease associated with a constellation of abnormalities including obesity, pigmentary retinopathy, polydactyly, renal abnormalities, learning disabilities, and hypogenitalism.

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}