ClinVar Miner

Submissions for variant NM_138713.4(NFAT5):c.2691A>G (p.Gln897=)

dbSNP: rs1567613850
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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 RCV001034921 SCV001198224 likely benign Immunodeficiency 2023-06-06 criteria provided, single submitter clinical testing

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