ClinVar Miner

Submissions for variant NM_001199267.2(DGKZ):c.162-910CCT[2]

dbSNP: rs750005398
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002154822 SCV002331434 benign not provided 2024-01-24 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002154822 SCV004130052 likely benign not provided 2023-04-01 criteria provided, single submitter clinical testing DGKZ: BS2

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