ClinVar Miner

Submissions for variant NM_033100.4(CDHR1):c.640-16T>C

gnomAD frequency: 0.02805  dbSNP: rs7073214
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000243258 SCV000315196 benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001519313 SCV001728158 benign not provided 2025-02-03 criteria provided, single submitter clinical testing
GeneDx RCV001519313 SCV001849003 benign not provided 2018-11-20 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001519313 SCV005317561 benign not provided criteria provided, single submitter not provided

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