{{Rsnum
|rsid=121964860
|Chromosome=1
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=TNNT2
|position=201361988
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TNNT2
}}{{omim
|id=191045
|rsnum=121964860
|variant=0009
}}{{ClinVar
|rsid=121964860
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=201361988
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000a05000002110100
|GENEINFO=TNNT2:7139
|GENE_NAME=TNNT2
|GENE_ID=7139
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.201361988C>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000364.3:c.635G>T; 191045.0009
|CLNSIG=5
|CLNCUI=C1832243
|CLNDBN=Left ventricular noncompaction 6
|Disease=Left ventricular noncompaction 6
|CLNACC=RCV000013228.23
|Tags=RV;PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1309:C1832243:601494:ORPHA154:ORPHA54260
}}