ClinVar Miner

Submissions for variant NM_024675.4(PALB2):c.1482T>C (p.Thr494=)

dbSNP: rs2142414557
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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 RCV002071697 SCV002424848 likely benign Familial cancer of breast 2021-11-15 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002508065 SCV002809507 likely benign Familial cancer of breast; Fanconi anemia complementation group N; Pancreatic cancer, susceptibility to, 3 2022-01-24 criteria provided, single submitter clinical testing

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