ClinVar Miner

Submissions for variant NM_024675.4(PALB2):c.2587-12C>T

gnomAD frequency: 0.00001  dbSNP: rs1266683395
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002079515 SCV002426328 likely benign Familial cancer of breast 2023-12-06 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002494346 SCV002798974 likely benign Familial cancer of breast; Fanconi anemia complementation group N; Pancreatic cancer, susceptibility to, 3 2022-05-06 criteria provided, single submitter clinical testing

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