{{Rsnum
|rsid=193922409
|Chromosome=19
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=TNNI3
|position=55151905
|Gene_s=TNNI3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922409
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=55663273
|CHROM=19
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050260000000000002100100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.55663273C>T
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Primary familial hypertrophic cardiomyopathy
|Disease=Primary familial hypertrophic cardiomyopathy
|Tags=RV;PM;S3D;OTHERKG;LSD
|CLNACC=RCV000030565.1
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1768:C0949658:83978005
|GENEINFO=TNNI3:7137
|GENE_ID=7137
|GENE_NAME=TNNI3
}}