ClinVar Miner

Submissions for variant NM_001166108.2(PALLD):c.2961C>T (p.Ile987=)

gnomAD frequency: 0.00002  dbSNP: rs1484758238
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001457711 SCV001661516 likely benign Pancreatic adenocarcinoma 2022-12-20 criteria provided, single submitter clinical testing

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