ClinVar Miner

Submissions for variant NM_199355.4(ADAMTS18):c.465C>T (p.Ser155=)

dbSNP: rs2057736782
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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 RCV002188048 SCV002353898 likely benign not provided 2024-07-30 criteria provided, single submitter clinical testing

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