ClinVar Miner

Submissions for variant NM_014339.7(IL17RA):c.33C>A (p.Val11=)

dbSNP: rs2123786594
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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 RCV001399919 SCV001601720 likely benign Immunodeficiency 51 2019-09-15 criteria provided, single submitter clinical testing

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