ClinVar Miner

Submissions for variant NM_001242896.3(DEPDC5):c.4204-6C>T

dbSNP: rs746382504
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002112859 SCV002396662 likely benign Familial focal epilepsy with variable foci 2024-06-11 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003426324 SCV004154908 likely benign not provided 2023-10-01 criteria provided, single submitter clinical testing DEPDC5: BP4

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