ClinVar Miner

Submissions for variant NM_139057.4(ADAMTS17):c.2022C>T (p.Ile674=)

gnomAD frequency: 0.00006  dbSNP: rs138584236
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 RCV000921323 SCV001066724 likely benign not provided 2024-11-04 criteria provided, single submitter clinical testing

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