ClinVar Miner

Submissions for variant NM_138713.4(NFAT5):c.3057G>A (p.Gln1019=)

dbSNP: rs2037605686
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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 RCV001469975 SCV001674065 likely benign Immunodeficiency 2020-02-27 criteria provided, single submitter clinical testing

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