ClinVar Miner

Submissions for variant NM_003954.5(MAP3K14):c.651A>G (p.Leu217=)

gnomAD frequency: 0.00004  dbSNP: rs766144092
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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 RCV000887024 SCV001030561 likely benign NIK deficiency 2024-01-24 criteria provided, single submitter clinical testing

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