ClinVar Miner

Submissions for variant NM_032444.4(SLX4):c.1900C>T (p.Leu634=)

dbSNP: rs768182554
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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 RCV001477929 SCV001682182 likely benign Fanconi anemia 2020-05-07 criteria provided, single submitter clinical testing

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