{{Rsnum
|rsid=137854887
|Chromosome=16
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=BBS2
|position=56510923
|Gene_s=BBS2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=137854887
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=56544835
|CHROM=16
|dbSNPBuildID=133
|SSR=0
|SAO=0
|VP=0x050068000000000002110100
|GENEINFO=BBS2:583
|GENE_NAME=BBS2
|GENE_ID=583
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.56544835T>C
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=606151.0018
|CLNSIG=5
|CLNCUI=C1970211; C1970211; C1970211; C1970211
|CLNDBN=Bardet-Biedl syndrome 2
|Disease=Bardet-Biedl syndrome 2
|CLNACC=RCV000023507.1
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen
|CLNDSDBID=NBK1363:C2936863
}}{{PMID Auto
|PMID=20618352
|Title=A founder mutation in BBS2 is responsible for Bardet-Biedl syndrome in the Hutterite population: utility of SNP arrays in genetically heterogeneous disorders.
}}