ClinVar Miner

Submissions for variant NM_138713.4(NFAT5):c.3378C>T (p.Ser1126=)

dbSNP: rs2151721671
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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 RCV002212525 SCV002370667 likely benign Immunodeficiency 2021-03-19 criteria provided, single submitter clinical testing

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