ClinVar Miner

Submissions for variant NM_138713.4(NFAT5):c.1053C>T (p.Asn351=)

gnomAD frequency: 0.00006  dbSNP: rs138688929
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000916162 SCV001061395 likely benign Immunodeficiency 2024-01-12 criteria provided, single submitter clinical testing

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