{{Rsnum
|rsid=74315379
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TNNT2
|position=201364336
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TNNT2
}}{{omim
|id=191045
|rsnum=74315379
|variant=0007
}}
{{omim
|id=191045
|rsnum=74315379
|variant=0008
}}{{ClinVar
|rsid=74315379
|Reversed=1
|FwdREF=C
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=201364336
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000b05000002110100
|GENEINFO=TNNT2:7139
|GENE_NAME=TNNT2
|GENE_ID=7139
|WGT=1
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000001.11:g.201364336G>A; NC_000001.11:g.201364336G>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000364.3:c.451C>T; 191045.0007; NM_000364.3:c.451C>A
|CLNSIG=5
|CLNCUI=C1832243
|CLNDBN=Left ventricular noncompaction 6; AllHighlyPenetrant
|Disease=Left ventricular noncompaction 6; AllHighlyPenetrant
|CLNACC=RCV000013225.22; RCV000036591.1
|Tags=RV;PM;NSM;REF;SYN;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet; MedGen
|CLNDSDBID=NBK1309:C1832243:601494:ORPHA154:ORPHA54260; CN169374
}}