ClinVar Miner

Submissions for variant NM_001166108.2(PALLD):c.*136G>A

dbSNP: rs752296365
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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 RCV000653485 SCV000775364 likely benign Pancreatic adenocarcinoma 2024-01-09 criteria provided, single submitter clinical testing

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