ClinVar Miner

Submissions for variant NM_032444.4(SLX4):c.4488C>T (p.Gly1496=)

dbSNP: rs2151121109
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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 RCV002151845 SCV002461399 likely benign Fanconi anemia 2023-12-09 criteria provided, single submitter clinical testing

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