ClinVar Miner

Submissions for variant NM_001384140.1(PCDH15):c.877-29G>T

gnomAD frequency: 0.01544  dbSNP: rs116339167
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000248115 SCV000315074 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001530603 SCV001745486 likely benign not provided 2018-08-23 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001530603 SCV005220773 likely benign not provided criteria provided, single submitter not provided

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