ClinVar Miner

Submissions for variant NM_153460.4(IL17RC):c.774G>C (p.Gln258His)

gnomAD frequency: 0.00303  dbSNP: rs115505677
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 RCV000652969 SCV000774842 benign Candidiasis, familial, 9 2024-01-12 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004708984 SCV005238668 benign not provided criteria provided, single submitter not provided

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