ClinVar Miner

Submissions for variant NM_003954.5(MAP3K14):c.2796C>T (p.Phe932=)

gnomAD frequency: 0.00001  dbSNP: rs781184920
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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 RCV002087284 SCV002330705 likely benign NIK deficiency 2023-11-03 criteria provided, single submitter clinical testing

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