ClinVar Miner

Submissions for variant NM_003283.6(TNNT1):c.795G>T (p.Arg265=) (rs890868)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001079399 SCV000641474 benign Nemaline myopathy 5 2020-12-01 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000024552 SCV001146216 benign not provided 2019-06-11 criteria provided, single submitter clinical testing
Leiden Muscular Dystrophy (TNNT1) RCV000024552 SCV000045856 not provided not provided 2012-03-18 no assertion provided curation

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