ClinVar Miner

Submissions for variant NM_153460.4(IL17RC):c.34C>T (p.Leu12=)

gnomAD frequency: 0.02548  dbSNP: rs7643547
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000652964 SCV000774837 benign Candidiasis, familial, 9 2024-01-29 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004708983 SCV005238661 benign not provided criteria provided, single submitter not provided
PreventionGenetics, part of Exact Sciences RCV003918084 SCV004731968 benign IL17RC-related disorder 2019-07-08 no assertion criteria provided clinical testing This variant is classified as benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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