ClinVar Miner

Submissions for variant NM_153460.4(IL17RC):c.1660C>G (p.Leu554Val)

gnomAD frequency: 0.00024  dbSNP: rs200293928
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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 RCV000960619 SCV001107619 benign Candidiasis, familial, 9 2023-12-09 criteria provided, single submitter clinical testing

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