ClinVar Miner

Submissions for variant NM_003954.5(MAP3K14):c.2502G>A (p.Gln834=)

dbSNP: rs2143767039
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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 RCV002202700 SCV002356787 likely benign NIK deficiency 2021-05-16 criteria provided, single submitter clinical testing

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