ClinVar Miner

Submissions for variant NM_014141.6(CNTNAP2):c.1854C>A (p.Gly618=)

dbSNP: rs61732849
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001413759 SCV001615879 likely benign Cortical dysplasia-focal epilepsy syndrome 2019-12-27 criteria provided, single submitter clinical testing

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