ClinVar Miner

Submissions for variant NM_001166108.2(PALLD):c.1965-12782C>A

dbSNP: rs2151117841
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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 RCV001486140 SCV001690590 likely benign Pancreatic adenocarcinoma 2023-10-20 criteria provided, single submitter clinical testing

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