ClinVar Miner

Submissions for variant NM_153460.4(IL17RC):c.877+7C>T

gnomAD frequency: 0.10691  dbSNP: rs11917994
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001522719 SCV001732312 benign Candidiasis, familial, 9 2024-01-31 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004709062 SCV005238671 benign not provided criteria provided, single submitter not provided

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