ClinVar Miner

Submissions for variant NM_001166108.2(PALLD):c.1965-12563C>T

dbSNP: rs2151120642
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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 RCV001414116 SCV001616243 likely benign Pancreatic adenocarcinoma 2020-10-22 criteria provided, single submitter clinical testing

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