ClinVar Miner

Submissions for variant NM_003954.5(MAP3K14):c.1839G>A (p.Pro613=)

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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 RCV003760483 SCV004540231 likely benign NIK deficiency 2023-06-20 criteria provided, single submitter clinical testing

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