ClinVar Miner

Submissions for variant NM_001166108.2(PALLD):c.3045G>A (p.Glu1015=)

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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 RCV003585561 SCV004267572 likely benign Pancreatic adenocarcinoma 2023-10-11 criteria provided, single submitter clinical testing

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