ClinVar Miner

Submissions for variant NM_014141.6(CNTNAP2):c.3716-7_3716-6insTT

dbSNP: rs72268642
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001704820 SCV000730574 benign not provided 2019-11-19 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000644739 SCV000766442 benign Cortical dysplasia-focal epilepsy syndrome 2025-01-20 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV000644739 SCV001821540 benign Cortical dysplasia-focal epilepsy syndrome 2021-07-22 criteria provided, single submitter clinical testing

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