ClinVar Miner

Submissions for variant NM_138713.4(NFAT5):c.2958A>G (p.Thr986=)

dbSNP: rs2151720409
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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 RCV001475326 SCV001679516 likely benign Immunodeficiency 2020-01-31 criteria provided, single submitter clinical testing

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