ClinVar Miner

Submissions for variant NM_016653.3(MAP3K20):c.1032+39G>A

gnomAD frequency: 0.26026  dbSNP: rs16861404
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001680126 SCV001899782 benign not provided 2021-05-17 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001776282 SCV002014228 benign Myopathy, centronuclear, 6, with fiber-type disproportion 2021-09-05 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001776281 SCV002014229 benign Split-foot malformation-mesoaxial polydactyly syndrome 2021-09-05 criteria provided, single submitter clinical testing

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