ClinVar Miner

Submissions for variant NM_032444.4(SLX4):c.4572C>T (p.Thr1524=)

gnomAD frequency: 0.00008  dbSNP: rs144666372
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001453696 SCV001657393 likely benign Fanconi anemia 2024-10-17 criteria provided, single submitter clinical testing

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