{{Rsnum
|rsid=80358250
|Chromosome=14
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CFL2
|position=34713462
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CFL2
}}{{omim
|id=601443
|rsnum=80358250
|variant=0001
}}{{ClinVar
|rsid=80358250
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=35182668
|CHROM=14
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=CFL2:1073
|GENE_NAME=CFL2
|GENE_ID=1073
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000014.8:g.35182668C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1288; 601443.0001
|CLNSIG=5
|CLNCUI=C1853154; C1853154
|CLNDBN=Nemaline myopathy 7
|Disease=Nemaline myopathy 7
|CLNACC=RCV000008638.2
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1288:C1853154:610687:607
}}{{PMID Auto
|PMID=17160903
|Title=Nemaline myopathy with minicores caused by mutation of the CFL2 gene encoding the skeletal muscle actin-binding protein, cofilin-2.
|OA=1
}}