ClinVar Miner

Submissions for variant NM_000283.4(PDE6B):c.2019C>T (p.Phe673=)

gnomAD frequency: 0.00001  dbSNP: rs959265084
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 RCV000917322 SCV001062597 likely benign not provided 2018-04-10 criteria provided, single submitter clinical testing

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