ClinVar Miner

Variants in gene combination TNNI3, TNNT1

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Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:

If a variant has more than one submission, it may be counted in more than one significance column. If this is the case, the total number of variants will be less than the sum of the other cells.

pathogenic likely pathogenic uncertain significance likely benign benign not provided total
2 0 1 3 3 2 6

Condition and significance breakdown #

Total conditions: 8
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Condition pathogenic uncertain significance likely benign benign not provided total
Nemaline myopathy 5 2 0 2 3 0 5
Hypertrophic cardiomyopathy 0 1 3 0 0 4
Dilated Cardiomyopathy, Recessive 0 0 3 0 0 3
Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome 0 0 3 0 0 3
Familial restrictive cardiomyopathy 0 0 3 0 0 3
not specified 0 0 1 3 0 3
Nemaline Myopathy, Recessive 0 0 2 0 0 2
not provided 0 0 0 0 2 2

Submitter and significance breakdown #

Total submitters: 9
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Submitter pathogenic uncertain significance likely benign benign not provided total
Invitae 1 1 0 2 0 4
GeneDx 0 0 0 3 0 3
Illumina Clinical Services Laboratory,Illumina 0 0 3 1 0 3
Genetic Services Laboratory, University of Chicago 0 0 1 1 0 2
Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine 0 0 0 2 0 2
PreventionGenetics,PreventionGenetics 0 0 0 2 0 2
Leiden Muscular Dystrophy (TNNT1) 0 0 0 0 2 2
Baylor Genetics 1 0 0 0 0 1
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics 0 0 0 1 0 1

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