ClinVar Miner

Submissions for variant NM_138713.4(NFAT5):c.2304A>G (p.Ala768=)

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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 RCV002588356 SCV003494334 likely benign Immunodeficiency 2022-07-09 criteria provided, single submitter clinical testing

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