ClinVar Miner

Submissions for variant NM_014494.4(TNRC6A):c.339_350del (p.113_114PQ[1])

dbSNP: rs71156436
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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 RCV000948974 SCV001095201 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001838648 SCV002098617 benign Epilepsy, familial adult myoclonic, 6 2021-09-10 criteria provided, single submitter clinical testing

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