ClinVar Miner

Submissions for variant NM_017563.5(IL17RD):c.185-13dup

dbSNP: rs142281539
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001592378 SCV001823967 likely benign not provided 2018-10-21 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001592378 SCV003031224 benign not provided 2025-01-13 criteria provided, single submitter clinical testing

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