ClinVar Miner

Submissions for variant NM_001166108.2(PALLD):c.2622+8A>G

dbSNP: rs2151306705
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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 RCV002183271 SCV002427939 likely benign Pancreatic adenocarcinoma 2021-09-15 criteria provided, single submitter clinical testing

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