ClinVar Miner

Submissions for variant NM_173660.5(DOK7):c.100+36del

dbSNP: rs566267525
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000248977 SCV000316508 likely benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001778874 SCV002015488 benign not provided 2021-11-11 criteria provided, single submitter clinical testing

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