ClinVar Miner

Submissions for variant NM_003611.3(OFD1):c.*3A>G

gnomAD frequency: 0.00113  dbSNP: rs183202009
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000712458 SCV000516470 benign not provided 2020-07-08 criteria provided, single submitter clinical testing
Athena Diagnostics RCV000712458 SCV000842956 benign not provided 2017-12-11 criteria provided, single submitter clinical testing

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