ClinVar Miner

Submissions for variant NM_014208.3(DSPP):c.136-33T>C

gnomAD frequency: 0.44289  dbSNP: rs13131929
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Total submissions: 7
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000252083 SCV000312093 benign not specified criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001660319 SCV001875761 benign Deafness, autosomal dominant 39, with dentinogenesis imperfecta 1 2021-07-30 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001660318 SCV001875762 benign Denticles 2021-07-30 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001660316 SCV001875763 benign Dentinogenesis imperfecta type 2 2021-07-30 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001660317 SCV001875764 benign Dentinogenesis imperfecta type 3 2021-07-30 criteria provided, single submitter clinical testing
GeneDx RCV001711713 SCV001939858 benign not provided 2018-11-11 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001711713 SCV005303232 benign not provided criteria provided, single submitter not provided

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