ClinVar Miner

Submissions for variant NM_138713.4(NFAT5):c.2373T>C (p.Asn791=)

dbSNP: rs1455036781
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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 RCV002166580 SCV002472530 likely benign Immunodeficiency 2022-09-01 criteria provided, single submitter clinical testing

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