ClinVar Miner

Submissions for variant NM_003611.3(OFD1):c.-296G>T (rs2285635)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001707513 SCV001934660 benign not provided 2018-06-26 criteria provided, single submitter clinical testing
GeneReviews RCV000034056 SCV000057986 non-pathogenic Orofaciodigital syndrome I 2013-02-28 no assertion criteria provided curation Converted during submission to Benign.

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