{{Rsnum
|rsid=80356516
|Chromosome=3
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=FLNB
|position=58145995
|Gene_s=FLNB
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=80356516
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=58131722
|CHROM=3
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=FLNB:2317
|GENE_NAME=FLNB
|GENE_ID=2317
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.58131722G>A
|CLNORIGIN=0
|CLNSIG=5
|CLNCUI=150250
|CLNDBN=Larsen syndrome, dominant type
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000020455.2
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK2534:C1835564:150250:503
|CLNSRC=GeneReviews
|CLNSRCID=NBK2534
|Disease=Larsen syndrome
}}{{PMID Auto
|PMID=16648377
|Title=Mutations responsible for Larsen syndrome cluster in the FLNB protein.
|OA=1
}}

{{PMID Auto
|PMID=16801345
|Title=A molecular and clinical study of Larsen syndrome caused by mutations in FLNB.
|OA=1
}}