{{Rsnum
|rsid=80356512
|Chromosome=3
|Orientation=plus
|geno1=(-;-)
|geno2=(-;AAT)
|geno3=(AAT;AAT)
|Gene=FLNB
|position=58136018
|Gene_s=FLNB
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=80356512
|Reversed=0
|FwdREF=AAT
|FwdALT=
|REF=CAAT
|ALT=C
|RSPOS=58121744
|CHROM=3
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050160000000000002110200
|GENEINFO=FLNB:2317
|GENE_NAME=FLNB
|GENE_ID=2317
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.58121745_58121747delAAT
|CLNORIGIN=0
|CLNSIG=5
|CLNCUI=150250
|CLNDBN=Larsen syndrome, dominant type
|Tags=PM;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000020446.2
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK2534:C1835564:150250:503
|CLNSRC=GeneReviews
|CLNSRCID=NBK2534
|Disease=Larsen syndrome
}}