ClinVar Miner

Submissions for variant NM_153460.4(IL17RC):c.186G>A (p.Ala62=)

gnomAD frequency: 0.00172  dbSNP: rs114515915
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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 RCV000893564 SCV001037508 benign Candidiasis, familial, 9 2024-01-06 criteria provided, single submitter clinical testing

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