ClinVar Miner

Submissions for variant NM_000363.4(TNNI3):c.-148A>G

gnomAD frequency: 0.00695  dbSNP: rs73935313
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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000370411 SCV000483803 likely benign Familial restrictive cardiomyopathy 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000275714 SCV000483804 likely benign Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000312062 SCV000483805 likely benign Dilated Cardiomyopathy, Recessive 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000366876 SCV000483806 likely benign Hypertrophic cardiomyopathy 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001580490 SCV001817720 likely benign not provided 2018-07-11 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001580490 SCV005206046 likely benign not provided criteria provided, single submitter not provided

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