ClinVar Miner

Submissions for variant NM_003611.3(OFD1):c.12+28G>C

gnomAD frequency: 0.00193  dbSNP: rs181620366
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000194256 SCV000248385 likely benign not specified 2015-08-05 criteria provided, single submitter clinical testing
GeneDx RCV001682911 SCV001903587 benign not provided 2020-03-14 criteria provided, single submitter clinical testing

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