{{Rsnum
|rsid=121917760
|Chromosome=19
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=TNNI3
|position=55154148
|Gene_s=TNNI3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=191044
|rsnum=121917760
|variant=0010
}}{{ClinVar
|rsid=121917760
|Reversed=1
|FwdREF=T
|FwdALT=A,C
|REF=A
|ALT=G,T
|RSPOS=55665516
|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.55665516A>G; NC_000019.9:g.55665516A>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=191044.0010
|CLNSIG=5
|CLNCUI=C1861861
|CLNDBN=Primary familial hypertrophic cardiomyopathy; Familial restrictive cardiomyopathy 1
|Disease=Primary familial hypertrophic cardiomyopathy; Familial restrictive cardiomyopathy 1
|CLNACC=RCV000036292.1; RCV000013241.21
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT; MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1768:C0949658:83978005; C1861861:115210:75249
}}