ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.1795-17A>T

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003792161 SCV004588367 likely benign Familial cancer of breast; Fanconi anemia complementation group J 2022-10-18 criteria provided, single submitter clinical testing

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