ClinVar Miner

Variants in gene combination DNAAF3, TNNI3, TNNT1

See also:
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 total
0 0 1 1 1 1

Condition and significance breakdown #

Total conditions: 10
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Condition uncertain significance likely benign benign total
Cardiomyopathy 1 0 1 1
Dilated cardiomyopathy 2A 0 0 1 1
Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome 0 0 1 1
Familial hypertrophic cardiomyopathy 7 0 0 1 1
Familial restrictive cardiomyopathy 1 0 0 1 1
Hypertrophic cardiomyopathy 0 0 1 1
Nemaline Myopathy, Recessive 0 1 0 1
Primary ciliary dyskinesia 0 0 1 1
Primary familial hypertrophic cardiomyopathy 0 0 1 1
not specified 0 1 1 1

Submitter and significance breakdown #

Total submitters: 8
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Submitter uncertain significance likely benign benign total
CHEO Genetics Diagnostic Laboratory,Children's Hospital of Eastern Ontario 1 0 0 1
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine 0 1 0 1
GeneDx 0 0 1 1
PreventionGenetics,PreventionGenetics 0 0 1 1
Women's Health and Genetics/Laboratory Corporation of America, LabCorp 0 0 1 1
Invitae 0 0 1 1
Illumina Clinical Services Laboratory,Illumina 0 1 1 1
Color Health, Inc 0 0 1 1

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