ClinVar Miner

Submissions for variant NM_001166108.2(PALLD):c.*109G>A

gnomAD frequency: 0.00002  dbSNP: rs1002500543
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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 RCV001492232 SCV001696839 likely benign Pancreatic adenocarcinoma 2023-07-17 criteria provided, single submitter clinical testing

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