ClinVar Miner

Submissions for variant NM_016653.3(MAP3K20):c.1360-28A>G

gnomAD frequency: 0.72578  dbSNP: rs820008
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001693152 SCV001911402 benign not provided 2021-05-16 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001776297 SCV002014230 benign Myopathy, centronuclear, 6, with fiber-type disproportion 2021-09-05 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001776296 SCV002014232 benign Split-foot malformation-mesoaxial polydactyly syndrome 2021-09-05 criteria provided, single submitter clinical testing

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