ClinVar Miner

Submissions for variant NM_003183.6(ADAM17):c.1915-146C>T

gnomAD frequency: 0.51347  dbSNP: rs883399
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001549058 SCV001769128 benign Inflammatory skin and bowel disease, neonatal, 1 2021-07-14 criteria provided, single submitter clinical testing
GeneDx RCV001713127 SCV001942551 benign not provided 2018-11-10 criteria provided, single submitter clinical testing

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