ClinVar Miner

Submissions for variant NM_032444.4(SLX4):c.278C>T (p.Thr93Ile)

dbSNP: rs2151139524
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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 RCV001898698 SCV002174224 uncertain significance Fanconi anemia 2021-09-01 criteria provided, single submitter clinical testing

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