ClinVar Miner

Submissions for variant NM_001166108.2(PALLD):c.2850+8T>G

dbSNP: rs2151424618
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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 RCV002139769 SCV002448446 likely benign Pancreatic adenocarcinoma 2022-03-07 criteria provided, single submitter clinical testing

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