ClinVar Miner

Submissions for variant NM_001572.5(IRF7):c.880A>T (p.Met294Leu)

dbSNP: rs1388076363
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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 RCV001925993 SCV002180843 uncertain significance Immunodeficiency 39 2021-08-28 criteria provided, single submitter clinical testing

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