ClinVar Miner

Submissions for variant NM_153460.4(IL17RC):c.105+24C>T

gnomAD frequency: 0.00042  dbSNP: rs192927730
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002065862 SCV002324096 benign Candidiasis, familial, 9 2021-10-02 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003923207 SCV004738003 likely benign IL17RC-related disorder 2019-09-17 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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