ClinVar Miner

Submissions for variant NM_014339.7(IL17RA):c.2522G>A (p.Arg841Gln)

gnomAD frequency: 0.00001  dbSNP: rs906456948
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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 RCV001040185 SCV001203746 uncertain significance Immunodeficiency 51 2021-09-01 criteria provided, single submitter clinical testing

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