ClinVar Miner

Submissions for variant NM_003954.5(MAP3K14):c.1291-9C>T

gnomAD frequency: 0.00001  dbSNP: rs191332614
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001498950 SCV001703705 likely benign NIK deficiency 2023-10-22 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004706228 SCV005212926 likely benign not provided criteria provided, single submitter not provided

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