ClinVar Miner

Submissions for variant NM_003954.5(MAP3K14):c.257-16A>C

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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 RCV002653754 SCV002979178 likely benign NIK deficiency 2021-12-13 criteria provided, single submitter clinical testing

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