ClinVar Miner

Submissions for variant NM_005076.5(CNTN2):c.2886C>T (p.His962=)

dbSNP: rs56111335
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 RCV000552586 SCV000654451 benign Epilepsy, familial adult myoclonic, 5 2024-02-01 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004714067 SCV005281758 benign not provided criteria provided, single submitter not provided

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