ClinVar Miner

Submissions for variant NM_003954.5(MAP3K14):c.2729G>A (p.Arg910His)

gnomAD frequency: 0.00001  dbSNP: rs367798756
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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 RCV001201670 SCV001372752 uncertain significance NIK deficiency 2021-08-27 criteria provided, single submitter clinical testing

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