ClinVar Miner

Submissions for variant NM_017777.4(MKS1):c.1407+66G>A

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Medical Genetics Center, Maternal and Child Health Hospital of Hubei Province RCV003219192 SCV003915599 uncertain significance Meckel syndrome, type 1 2021-03-19 criteria provided, single submitter clinical testing

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