ClinVar Miner

Submissions for variant NM_003954.5(MAP3K14):c.1134G>A (p.Glu378=)

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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 RCV003595321 SCV004276400 likely benign NIK deficiency 2023-01-22 criteria provided, single submitter clinical testing

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