ClinVar Miner

Submissions for variant NM_000787.4(DBH):c.1539G>A (p.Gln513=)

gnomAD frequency: 0.00605  dbSNP: rs78516399
Minimum review status: Collection method:
Minimum conflict level:
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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 RCV000974738 SCV001122591 benign Orthostatic hypotension 1 2025-01-29 criteria provided, single submitter clinical testing

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