ClinVar Miner

Submissions for variant NM_032444.4(SLX4):c.3081A>T (p.Ala1027=)

dbSNP: rs2151124384
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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 RCV002156789 SCV002330784 likely benign Fanconi anemia 2021-04-06 criteria provided, single submitter clinical testing

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