ClinVar Miner

Variants in gene 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
11 5 74 61 27 10 163

Condition and significance breakdown #

Total conditions: 5
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Condition pathogenic likely pathogenic uncertain significance likely benign benign not provided total
Nemaline myopathy 5 7 5 69 27 7 0 110
not provided 4 0 3 26 18 10 55
not specified 0 0 1 18 6 0 24
Nemaline Myopathy, Recessive 0 0 2 0 0 0 2
Inborn genetic diseases 0 0 1 0 0 0 1

Submitter and significance breakdown #

Total submitters: 18
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign not provided total
Invitae 6 3 54 27 6 0 96
GeneDx 0 0 1 34 20 0 55
Illumina Clinical Services Laboratory,Illumina 0 0 20 1 1 0 22
PreventionGenetics,PreventionGenetics 0 0 0 5 5 0 10
Leiden Muscular Dystrophy (TNNT1) 0 0 0 0 0 10 10
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics 2 0 2 0 2 0 6
Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine 0 0 0 0 3 0 3
Baylor Genetics 0 0 2 0 0 0 2
Genetic Services Laboratory, University of Chicago 0 0 1 1 0 0 2
Pediatric Department, Peking University First Hospital 1 1 0 0 0 0 2
CeGaT Praxis fuer Humangenetik Tuebingen 1 0 1 0 0 0 2
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen 1 0 0 0 1 0 2
OMIM 1 0 0 0 0 0 1
Athena Diagnostics Inc 0 0 0 0 1 0 1
Ambry Genetics 0 0 1 0 0 0 1
Genome Diagnostics Laboratory,University Medical Center Utrecht 0 0 0 0 1 0 1
GeneReviews 1 0 0 0 0 0 1
Hadassah Hebrew University Medical Center 0 1 0 0 0 0 1

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