ClinVar Miner

Submissions for variant NM_138713.4(NFAT5):c.1775-20T>C

dbSNP: rs200979203
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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 RCV002174853 SCV002342586 benign Immunodeficiency 2024-11-04 criteria provided, single submitter clinical testing

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