ClinVar Miner

Submissions for variant NM_003954.5(MAP3K14):c.1205A>G (p.His402Arg)

gnomAD frequency: 0.00002  dbSNP: rs753326951
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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 RCV001344651 SCV001538717 uncertain significance NIK deficiency 2021-09-01 criteria provided, single submitter clinical testing

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