ClinVar Miner

Submissions for variant NM_001166108.2(PALLD):c.2199+18A>G

gnomAD frequency: 0.00001  dbSNP: rs1754743835
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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 RCV003037165 SCV003439360 likely benign Pancreatic adenocarcinoma 2023-12-06 criteria provided, single submitter clinical testing

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