ClinVar Miner

Submissions for variant NM_003183.6(ADAM17):c.958-13del

dbSNP: rs34863481
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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
GeneDx RCV001714939 SCV001938913 benign not provided 2021-06-09 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002073326 SCV002402879 benign Inflammatory skin and bowel disease, neonatal, 1 2025-01-13 criteria provided, single submitter clinical testing

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