ClinVar Miner

Submissions for variant NM_001572.5(IRF7):c.340G>A (p.Asp114Asn)

dbSNP: rs758401823
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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 RCV001225733 SCV001398022 uncertain significance Immunodeficiency 39 2021-08-31 criteria provided, single submitter clinical testing

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