{{Rsnum
|rsid=80356513
|Chromosome=3
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=FLNB
|position=58136063
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FLNB
}}{{omim
|id=603381
|rsnum=80356513
|variant=0005
}}{{ClinVar
|rsid=80356513
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=58121790
|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.58121790G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK2534; 603381.0005
|CLNSIG=5
|CLNCUI=C1835564
|CLNDBN=Larsen syndrome; Larsen syndrome, dominant type
|Disease=Larsen syndrome; Larsen syndrome
|CLNACC=RCV000030661.1; RCV000030669.2
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:SNOMED_CT; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=C0175778:63387002; NBK2534:C1835564:150250:503
}}{{PMID Auto
|PMID=14991055
|Title=Mutations in the gene encoding filamin B disrupt vertebral segmentation, joint formation and skeletogenesis.
}}