{{Rsnum
|rsid=267607126
|Chromosome=3
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=TNNC1
|position=52451810
|Gene_s=TNNC1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=3
|CLNACC=RCV000013257.1
|CLNALLE=1
|CLNDBN=Familial hypertrophic cardiomyopathy 13
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C2750472:613243
|CLNHGVS=NC_000003.11:g.52485826C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=191040.0004
|Disease=Familial hypertrophic cardiomyopathy 13
|FwdALT=A
|FwdREF=G
|GENEINFO=TNNC1:7134
|GENE_ID=7134
|GENE_NAME=TNNC1
|REF=C
|RSPOS=52485826
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;S3D;NSM;REF;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000a01000002110100
|WGT=1
|dbSNPBuildID=137
|rsid=267607126
}}