ClinVar Miner

Submissions for variant NM_018699.4(PRDM5):c.178-18G>T

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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 RCV003848445 SCV004694003 likely benign not provided 2024-01-09 criteria provided, single submitter clinical testing

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