ClinVar Miner

Submissions for variant NM_138713.4(NFAT5):c.3894G>T (p.Ala1298=)

dbSNP: rs528549177
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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 RCV001464292 SCV001668258 likely benign Immunodeficiency 2020-09-08 criteria provided, single submitter clinical testing

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