ClinVar Miner

Submissions for variant NM_000038.6(APC):c.1627-93A>C

gnomAD frequency: 0.00999  dbSNP: rs115157960
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
GeneDx RCV001558282 SCV001780195 likely benign not provided 2018-06-28 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001558282 SCV005226824 likely benign not provided criteria provided, single submitter not provided
Mayo Clinic Laboratories, Mayo Clinic RCV000202116 SCV000256927 benign not specified no assertion criteria provided research

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