ClinVar Miner

Submissions for variant NM_000787.4(DBH):c.789C>T (p.His263=)

dbSNP: rs2131285657
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001398265 SCV001600033 likely benign Orthostatic hypotension 1 2020-08-22 criteria provided, single submitter clinical testing

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