ClinVar Miner

Submissions for variant NM_003611.3(OFD1):c.935+595A>G

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003441019 SCV004166541 likely benign not provided 2023-01-01 criteria provided, single submitter clinical testing OFD1: BS2

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