ClinVar Miner

Submissions for variant NM_003283.6(TNNT1):c.-12+30T>C

gnomAD frequency: 0.22105  dbSNP: rs28362592
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000024559 SCV001900788 benign not provided 2019-04-11 criteria provided, single submitter clinical testing
Leiden Muscular Dystrophy (TNNT1) RCV000024559 SCV000045863 not provided not provided 2012-03-18 no assertion provided curation

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