ClinVar Miner

Submissions for variant NM_138713.4(NFAT5):c.2262G>A (p.Glu754=)

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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 RCV005146924 SCV005781371 likely benign Immunodeficiency 2024-08-02 criteria provided, single submitter clinical testing

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