ClinVar Miner

Submissions for variant NM_014141.6(CNTNAP2):c.551-15_551-14insG

gnomAD frequency: 0.00247 dbSNP: rs201428458

Minimum review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total submissions: 1

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Labcorp Genetics (formerly Invitae), Labcorp	RCV002124642	SCV002408765	benign	Cortical dysplasia-focal epilepsy syndrome	2025-01-15	criteria provided, single submitter	clinical testing

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