{{Rsnum
|rsid=104894727
|Chromosome=19
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=TNNI3
|position=55151881
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TNNI3
}}{{omim
|id=191044
|rsnum=104894727
|variant=0004
}}{{ClinVar
|rsid=104894727
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=55663249
|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
|CLNHGVS=NC_000019.9:g.55663249C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=191044.0004
|CLNSIG=5
|CLNCUI=CN069699
|CLNDBN=Familial hypertrophic cardiomyopathy 7; AllHighlyPenetrant
|Disease=Familial hypertrophic cardiomyopathy 7; AllHighlyPenetrant
|CLNACC=RCV000013234.21; RCV000036308.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM; MedGen
|CLNDSDBID=CN069699:613690; CN169374
}}