ClinVar Miner

Submissions for variant NM_024411.5(PDYN):c.607C>T (p.Leu203=)

gnomAD frequency: 0.00001  dbSNP: rs1185514961
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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 RCV000971829 SCV001119499 likely benign not provided 2017-08-09 criteria provided, single submitter clinical testing

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