ClinVar Miner

Submissions for variant NM_006258.4(PRKG1):c.834A>G (p.Lys278=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003582718 SCV004305194 likely benign Aortic aneurysm, familial thoracic 8 2023-06-16 criteria provided, single submitter clinical testing

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