{{Rsnum
|rsid=121909518
|Chromosome=7
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=FLNC
|position=128858475
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FLNC
}}{{omim
|id=102565
|rsnum=121909518
|variant=0001
}}{{ClinVar
|rsid=121909518
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=128498529
|CHROM=7
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=FLNC:2318
|GENE_NAME=FLNC
|GENE_ID=2318
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.128498529G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=102565.0001
|CLNSIG=5
|CLNCUI=C1836050
|CLNDBN=Myofibrillar myopathy, filamin C-related
|Disease=Myofibrillar myopathy
|CLNACC=RCV000019978.27
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1499:C1836050:609524
}}