ClinVar Miner

Submissions for variant NM_032444.4(SLX4):c.2854_2855delinsAT (p.Ala952Met) (rs863224277)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000199487 SCV000252879 benign Fanconi anemia 2018-01-16 criteria provided, single submitter clinical testing
Vantari Genetics RCV000210791 SCV000267091 likely benign Hereditary cancer-predisposing syndrome 2015-12-07 criteria provided, single submitter clinical testing

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