ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.44005G>A (p.Asp14669Asn)

dbSNP: rs2471412597
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Genetics, Labor Dr. Heidrich & Kollegen MVZ GmbH RCV003307377 SCV004009616 uncertain significance not provided 2023-06-15 no assertion criteria provided clinical testing

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