ClinVar Miner

Submissions for variant NM_000283.4(PDE6B):c.1959C>T (p.His653=)

gnomAD frequency: 0.00006  dbSNP: rs141521651
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 RCV001443295 SCV001646264 likely benign not provided 2023-07-17 criteria provided, single submitter clinical testing

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