ClinVar Miner

Submissions for variant NM_018444.4(PDP1):c.546C>T (p.Ser182=)

gnomAD frequency: 0.00006  dbSNP: rs202034256
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001571695 SCV001796208 likely benign not provided 2021-01-07 criteria provided, single submitter clinical testing
Invitae RCV001571695 SCV003293703 likely benign not provided 2023-07-25 criteria provided, single submitter clinical testing

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