ClinVar Miner

Submissions for variant NM_014339.7(IL17RA):c.18C>T (p.Ser6=)

gnomAD frequency: 0.00001  dbSNP: rs988752151
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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 RCV001409490 SCV001611514 likely benign Immunodeficiency 51 2023-06-15 criteria provided, single submitter clinical testing

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