{{Rsnum
|rsid=121964855
|Chromosome=1
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=TNNT2
|position=201365638
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TNNT2
}}{{omim
|id=191045
|rsnum=121964855
|variant=0001
}}{{ClinVar
|rsid=121964855
|Reversed=1
|FwdREF=T
|FwdALT=A
|REF=A
|ALT=T
|RSPOS=201365638
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000a05000002110100
|GENEINFO=TNNT2:7139
|GENE_NAME=TNNT2
|GENE_ID=7139
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.201365638A>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000364.3:c.266T>A; 191045.0001
|CLNSIG=5
|CLNCUI=C1861864; C1832243; C2676271
|CLNDBN=Familial hypertrophic cardiomyopathy 2; Left ventricular noncompaction 6; Familial restrictive cardiomyopathy 3; Primary familial hypertrophic cardiomyopathy
|Disease=Familial hypertrophic cardiomyopathy 2; Left ventricular noncompaction 6; Familial restrictive cardiomyopathy 3; Primary familial hypertrophic cardiomyopathy
|CLNACC=RCV000013217.23; RCV000013218.15; RCV000013219.22; RCV000036564.1
|Tags=RV;PM;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM; GeneReviews:MedGen:OMIM:Orphanet:Orphanet; MedGen:OMIM:Orphanet; GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1768:C1861864:115195; NBK1309:C1832243:601494:ORPHA154:ORPHA54260; C2676271:612422:ORPHA75249; NBK1768:C0949658:83978005
}}