ClinVar Miner

Submissions for variant NM_024675.4:c.3179_3180insALU

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005022307 SCV005646461 likely pathogenic Fanconi anemia complementation group N; Pancreatic cancer, susceptibility to, 3; Breast-ovarian cancer, familial, susceptibility to, 5 2024-03-12 criteria provided, single submitter clinical testing

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