{{Rsnum
|rsid=199469665
|Chromosome=2
|Orientation=minus
|geno1=(-;-)
|geno2=(-;ACCAAGTG)
|geno3=(ACCAAGTG;ACCAAGTG)
|Gene=TTN
|position=178531084
|Gene_s=LGR4,TTN
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=199469665
|Reversed=1
|FwdREF=CCAAGTGA
|FwdALT=
|REF=TCACTTGGT
|ALT=T
|RSPOS=179395810
|CHROM=2
|dbSNPBuildID=136
|SSR=0
|SAO=0
|VP=0x050368000000000002110200
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.179395811_179395818delCACTTGGT
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK83297; 188840.0013
|CLNSIG=5
|CLNCUI=C2673677
|CLNDBN=Myopathy, early-onset, with fatal cardiomyopathy
|Disease=Myopathy
|CLNACC=RCV000013497.21
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK83297:C2673677:611705:289377
|GENEINFO=TTN:7273; TTN-AS1:100506866
|GENE_ID=7273; 100506866
|GENE_NAME=TTN; TTN-AS1
}}{{PMID Auto
|PMID=17444505
|Title=C-terminal titin deletions cause a novel early-onset myopathy with fatal cardiomyopathy.
}}