{{Rsnum
|rsid=267607125
|Chromosome=3
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TNNC1
|position=52453993
|Gene_s=NISCH,TNNC1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=3
|CLNACC=RCV000013256.22; RCV000037762.1
|CLNALLE=1
|CLNDBN=Familial hypertrophic cardiomyopathy 13; AllHighlyPenetrant
|CLNDSDB=MedGen:OMIM; MedGen
|CLNDSDBID=C2750472:613243; CN169374
|CLNHGVS=NC_000003.11:g.52488009G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=191040.0003
|Disease=Familial hypertrophic cardiomyopathy 13; AllHighlyPenetrant
|FwdALT=T
|FwdREF=C
|GENEINFO=TNNC1:7134; NISCH:11188
|GENE_ID=7134; 11188
|GENE_NAME=TNNC1; NISCH
|REF=G
|RSPOS=52488009
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267607125
}}