ClinVar Miner

Submissions for variant NM_138713.4(NFAT5):c.1775-18G>T

dbSNP: rs377188619
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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 RCV002200268 SCV002355619 likely benign Immunodeficiency 2023-11-03 criteria provided, single submitter clinical testing

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