ClinVar Miner

Submissions for variant NM_199355.4(ADAMTS18):c.1711-10C>T

gnomAD frequency: 0.00001  dbSNP: rs372315599
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001406764 SCV001608720 likely benign not provided 2022-02-02 criteria provided, single submitter clinical testing

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