ClinVar Miner

Submissions for variant NM_006785.4(MALT1):c.1401-15G>T

dbSNP: rs371051170
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV001333584 SCV001526213 uncertain significance Combined immunodeficiency due to MALT1 deficiency 2018-01-13 criteria provided, single submitter clinical testing This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].
Labcorp Genetics (formerly Invitae), Labcorp RCV001333584 SCV003515455 likely benign Combined immunodeficiency due to MALT1 deficiency 2024-07-10 criteria provided, single submitter clinical testing

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