ClinVar Miner

Submissions for variant NM_006785.4(MALT1):c.1754-15A>T

dbSNP: rs2144488842
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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 RCV002138008 SCV002459949 likely benign Combined immunodeficiency due to MALT1 deficiency 2021-03-09 criteria provided, single submitter clinical testing

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