ClinVar Miner

Submissions for variant NM_003954.5(MAP3K14):c.1720G>A (p.Asp574Asn)

dbSNP: rs996613711
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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 RCV000698152 SCV000826796 uncertain significance NIK deficiency 2021-08-28 criteria provided, single submitter clinical testing

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