ClinVar Miner

Submissions for variant NM_016653.3(MAP3K20):c.670-11G>C

gnomAD frequency: 0.98158  dbSNP: rs11899707
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001534663 SCV001751598 benign not provided 2020-02-19 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001776254 SCV002014226 benign Myopathy, centronuclear, 6, with fiber-type disproportion 2021-09-05 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001776253 SCV002014227 benign Split-foot malformation-mesoaxial polydactyly syndrome 2021-09-05 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001534663 SCV002481567 benign not provided 2025-02-03 criteria provided, single submitter clinical testing

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