ClinVar Miner

Submissions for variant NM_006258.4(PRKG1):c.652A>C (p.Arg218=)

dbSNP: rs2132611314
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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 RCV001496070 SCV001700761 likely benign Aortic aneurysm, familial thoracic 8 2020-05-21 criteria provided, single submitter clinical testing

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