{{Rsnum
|rsid=77615401
|Gene=TNNI3
|Chromosome=19
|position=55156239
|Orientation=plus
|GMAF=0.003214
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=TNNI3
}}{{omim
|id=191044
|rsnum=77615401
|variant=0003
}}{{ClinVar
|rsid=77615401
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=55667607
|CHROM=19
|GMAF=0.0032
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050260000000040416110100
|GENEINFO=TNNI3:7137
|GENE_NAME=TNNI3
|GENE_ID=7137
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.55667607G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=191044.0003
|CLNSIG=5
|CLNCUI=CN069699
|CLNDBN=Familial hypertrophic cardiomyopathy 7; AllHighlyPenetrant
|Disease=Familial hypertrophic cardiomyopathy 7; AllHighlyPenetrant
|CLNACC=RCV000013233.22; RCV000036277.1
|Tags=PM;S3D;VLD;HD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9968; 0.003214
|CLNDSDB=MedGen:OMIM; MedGen
|CLNDSDBID=CN069699:613690; CN169374
|COMMON=1
}}