ClinVar Miner

Submissions for variant NM_138713.4(NFAT5):c.1369+16C>T

dbSNP: rs370755900
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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 RCV002220896 SCV002364689 benign Immunodeficiency 2023-12-28 criteria provided, single submitter clinical testing

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