{{Rsnum
|rsid=80356521
|Chromosome=3
|Orientation=plus
|geno1=(-;-)
|geno2=(-;C)
|geno3=(C;C)
|Gene=FLNB
|position=58153415
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FLNB
}}{{omim
|id=603381
|rsnum=80356521
|variant=0001
}}{{ClinVar
|rsid=80356521
|Reversed=0
|FwdREF=C
|FwdALT=
|REF=GC
|ALT=G
|RSPOS=58139138
|CHROM=3
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000000000002110200
|GENEINFO=FLNB:2317
|GENE_NAME=FLNB
|GENE_ID=2317
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.58139142delC
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK2534; 603381.0001
|CLNSIG=5
|CLNCUI=C1848934; C1848934
|CLNDBN=Spondylocarpotarsal synostosis syndrome
|Disease=Spondylocarpotarsal synostosis syndrome
|CLNACC=RCV000006767.2
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK2534:C1848934:272460:3275
}}{{PMID Auto
|PMID=14991055
|Title=Mutations in the gene encoding filamin B disrupt vertebral segmentation, joint formation and skeletogenesis.
}}