{{Rsnum
|rsid=397516456
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TNNT2
|position=201365298
|Gene_s=TNNT2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=1
|CLNACC=RCV000036573.1
|CLNALLE=1
|CLNDBN=Primary familial hypertrophic cardiomyopathy
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1768:C0949658:83978005
|CLNHGVS=NC_000001.11:g.201365298G>A
|CLNSIG=5
|Disease=Primary familial hypertrophic cardiomyopathy
|FwdALT=T
|FwdREF=C
|GENEINFO=TNNT2:7139
|GENE_ID=7139
|GENE_NAME=TNNT2
|REF=G
|RSPOS=201365298
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;NSM;REF;INT;ASP;OTHERKG;LSD
|VC=SNV
|VP=0x050060080a05000002100100
|WGT=1
|dbSNPBuildID=138
|rsid=397516456
|CLNORIGIN=1
|CLNSRC=ClinVar
|CLNSRCID=NM_000364.3:c.304C>T; NM_001276346.1:c.291+312C>T
}}