ClinVar Miner

Submissions for variant NM_006258.4(PRKG1):c.1174-9T>G

gnomAD frequency: 0.00008  dbSNP: rs372515971
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000230575 SCV000289505 likely benign Aortic aneurysm, familial thoracic 8 2025-01-15 criteria provided, single submitter clinical testing
GeneDx RCV001697680 SCV000725156 likely benign not provided 2020-01-16 criteria provided, single submitter clinical testing

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