ClinVar Miner

Submissions for variant NM_001166108.2(PALLD):c.*124C>T

gnomAD frequency: 0.00002  dbSNP: rs369747738
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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 RCV002205245 SCV002361137 likely benign Pancreatic adenocarcinoma 2024-01-10 criteria provided, single submitter clinical testing

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