ClinVar Miner

Submissions for variant NM_024675.4(PALB2):c.212-16dup

dbSNP: rs766487430
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001517220 SCV001725671 benign Familial cancer of breast 2024-09-03 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV001524670 SCV001734602 likely benign Hereditary cancer-predisposing syndrome 2020-10-12 criteria provided, single submitter clinical testing

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