ClinVar Miner

Submissions for variant NM_138713.4(NFAT5):c.2793A>G (p.Ser931=)

dbSNP: rs2037592859
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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 RCV001411587 SCV001613650 likely benign Immunodeficiency 2020-07-07 criteria provided, single submitter clinical testing

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