ClinVar Miner

Submissions for variant NM_005120.3(MED12):c.4416-77CTCTT[13]

dbSNP: rs56658066
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000081263 SCV000113171 uncertain significance not provided 2014-05-14 criteria provided, single submitter clinical testing
GeneDx RCV000081263 SCV001944268 benign not provided 2019-11-19 criteria provided, single submitter clinical testing

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