ClinVar Miner

Submissions for variant NM_053025.4(MYLK):c.4289-4C>A

dbSNP: rs376670657
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000841603 SCV000983574 likely benign not provided 2020-10-29 criteria provided, single submitter clinical testing
Invitae RCV003525965 SCV004299673 likely benign Aortic aneurysm, familial thoracic 7 2024-01-05 criteria provided, single submitter clinical testing

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