{{Rsnum
|rsid=104894724
|Chromosome=19
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=TNNI3
|position=55154146
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TNNI3
}}{{omim
|id=191044
|rsnum=104894724
|variant=0001
}}
{{omim
|id=191044
|rsnum=104894724
|variant=0008
}}{{ClinVar
|rsid=104894724
|Reversed=1
|FwdREF=C
|FwdALT=G,T
|REF=G
|ALT=A,C
|RSPOS=55665514
|CHROM=19
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=TNNI3:7137
|GENE_NAME=TNNI3
|GENE_ID=7137
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000019.9:g.55665514G>A; NC_000019.9:g.55665514G>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=191044.0008; 191044.0001
|CLNSIG=5
|CLNCUI=C1861861; CN069699
|CLNDBN=Familial restrictive cardiomyopathy 1; Primary familial hypertrophic cardiomyopathy; Familial hypertrophic cardiomyopathy 7
|Disease=Familial restrictive cardiomyopathy 1; Primary familial hypertrophic cardiomyopathy; Familial hypertrophic cardiomyopathy 7
|CLNACC=RCV000013239.21; RCV000036294.1; RCV000013231.21; RCV000036293.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet; GeneReviews:MedGen:SNOMED_CT; MedGen:OMIM
|CLNDSDBID=C1861861:115210:75249; NBK1768:C0949658:83978005; CN069699:613690
}}