{{Rsnum
|rsid=121964856
|Chromosome=1
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=TNNT2
|position=201365297
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TNNT2
}}{{omim
|id=191045
|rsnum=121964856
|variant=0002
}}{{ClinVar
|rsid=121964856
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=201365297
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060080a05000002110100
|GENEINFO=TNNT2:7139
|GENE_NAME=TNNT2
|GENE_ID=7139
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.201365297C>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000364.3:c.305G>A; NM_001276346.1:c.291+313G>A; 191045.0002
|CLNSIG=5
|CLNCUI=C1861864
|CLNDBN=Familial hypertrophic cardiomyopathy 2; Primary familial hypertrophic cardiomyopathy
|Disease=Familial hypertrophic cardiomyopathy 2; Primary familial hypertrophic cardiomyopathy
|CLNACC=RCV000013220.15; RCV000036574.1
|Tags=RV;PM;NSM;REF;INT;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM; GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1768:C1861864:115195; NBK1768:C0949658:83978005
}}