ClinVar Miner

Submissions for variant NM_003611.3(OFD1):c.1654+5G>C

dbSNP: rs1555906316
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV001815336 SCV000596161 likely pathogenic not provided 2021-04-09 criteria provided, single submitter clinical testing

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