ClinVar Miner

Submissions for variant NM_003954.5(MAP3K14):c.656dup (p.Ala220fs)

dbSNP: rs56405343
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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 RCV001523211 SCV001732883 benign NIK deficiency 2024-02-01 criteria provided, single submitter clinical testing

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