{{Rsnum
|rsid=121964857
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TNNT2
|position=201359245
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TNNT2
}}{{omim
|id=191045
|rsnum=121964857
|variant=0004
}}{{ClinVar
|rsid=121964857
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=201359245
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000a05040002110100
|GENEINFO=TNNT2:7139
|GENE_NAME=TNNT2
|GENE_ID=7139
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.201359245G>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000364.3:c.853C>T; 191045.0004
|CLNSIG=5
|CLNCUI=C1861864
|CLNDBN=Familial hypertrophic cardiomyopathy 2; AllHighlyPenetrant
|Disease=Familial hypertrophic cardiomyopathy 2; AllHighlyPenetrant
|CLNACC=RCV000013222.22; RCV000036622.1
|Tags=RV;PM;S3D;NSM;REF;ASP;VLD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM; MedGen
|CLNDSDBID=NBK1768:C1861864:115195; CN169374
}}