ClinVar Miner

Submissions for variant NM_032444.4(SLX4):c.2481G>A (p.Glu827=)

dbSNP: rs746049343
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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 RCV001404194 SCV001606090 likely benign Fanconi anemia 2023-11-27 criteria provided, single submitter clinical testing

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