ClinVar Miner

Submissions for variant NM_032444.4(SLX4):c.1366+7G>A

gnomAD frequency: 0.00001  dbSNP: rs199889969
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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 RCV002135410 SCV002459009 likely benign Fanconi anemia 2024-01-22 criteria provided, single submitter clinical testing

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