ClinVar Miner

Submissions for variant NM_138713.4(NFAT5):c.1569T>C (p.Ile523=)

dbSNP: rs2151685989
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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 RCV001504328 SCV001709204 likely benign Immunodeficiency 2019-12-19 criteria provided, single submitter clinical testing

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