ClinVar Miner

Submissions for variant NM_001166108.2(PALLD):c.2101-10C>T

gnomAD frequency: 0.00002  dbSNP: rs757885388
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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 RCV001478088 SCV001682346 likely benign Pancreatic adenocarcinoma 2024-09-23 criteria provided, single submitter clinical testing

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