ClinVar Miner

Submissions for variant NM_199355.4(ADAMTS18):c.1473G>A (p.Ala491=)

gnomAD frequency: 0.00002  dbSNP: rs148669189
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001400832 SCV001602643 likely benign not provided 2024-02-24 criteria provided, single submitter clinical testing

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