ClinVar Miner

Submissions for variant NM_024675.4(PALB2):c.48+10dup

dbSNP: rs1567225760
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000776653 SCV000912275 likely benign Hereditary cancer-predisposing syndrome 2017-10-12 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003500594 SCV004249202 benign Familial cancer of breast 2024-06-15 criteria provided, single submitter clinical testing

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