{{Rsnum
|rsid=74315380
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TNNT2
|position=201364366
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TNNT2
}}{{omim
|id=191045
|rsnum=74315380
|variant=0007
}}
{{omim
|id=191045
|rsnum=74315380
|variant=0008
}}{{ClinVar
|rsid=74315380
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=201364366
|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.201364366G>A
|CLNSRC=ClinVar; LabCorp; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000364.3:c.421C>T; NM_001001432.1:c.376C>T; 191045.0008
|CLNSIG=5
|CLNCUI=C1832243; CN043473
|CLNACC=RCV000013226.22; RCV000030567.1; RCV000036584.1
|Tags=RV;PM;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDBN=Left ventricular noncompaction 6; Primary dilated cardiomyopathy; AllHighlyPenetrant
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet; GeneReviews:MedGen:OMIM:SNOMED_CT; MedGen
|CLNDSDBID=NBK1309:C1832243:601494:ORPHA154:ORPHA54260; NBK1309:C0007193:212110:195021004; CN169374
|Disease=Left ventricular noncompaction 6; Primary dilated cardiomyopathy; AllHighlyPenetrant
}}