ClinVar Miner

Submissions for variant NM_004366.6(CLCN2):c.773-9C>G

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002886301 SCV003246909 likely benign not provided 2024-10-11 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005034455 SCV005665098 uncertain significance Epilepsy, idiopathic generalized, susceptibility to, 11; Familial hyperaldosteronism type II; Leukoencephalopathy with mild cerebellar ataxia and white matter edema 2024-01-04 criteria provided, single submitter clinical testing

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