ClinVar Miner

Submissions for variant NM_199355.4(ADAMTS18):c.1057-3T>C

gnomAD frequency: 0.00001  dbSNP: rs552066778
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002157552 SCV002340147 likely benign not provided 2024-12-09 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV002157552 SCV005219193 likely benign not provided criteria provided, single submitter not provided

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