{{Rsnum
|rsid=111377893
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=TNNT2
|position=201359622
|Gene_s=TNNT2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G,T
|CHROM=1
|CLNACC=RCV000036621.1
|CLNALLE=2
|CLNDBN=Primary familial hypertrophic cardiomyopathy
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1768:C0949658:83978005
|CLNHGVS=NC_000001.11:g.201359622C>T
|CLNSIG=5
|Disease=Primary familial hypertrophic cardiomyopathy
|FwdALT=G,T
|FwdREF=C
|GENEINFO=TNNT2:7139
|GENE_ID=7139
|GENE_NAME=TNNT2
|REF=C
|RSPOS=201359622
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;SLO;DSS;OTH;ASP;HD;GNO;OTHERKG;LSD
|VC=SNV
|VP=0x050160100015000502100100
|WGT=1
|dbSNPBuildID=132
|rsid=111377893
|CLNORIGIN=1
|CLNSRC=ClinVar
|CLNSRCID=NM_000364.3:c.842+1G>A
}}