ClinVar Miner

Submissions for variant NM_052872.4(IL17F):c.462C>T (p.Cys154=)

gnomAD frequency: 0.00001  dbSNP: rs780312510
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002092571 SCV002332876 likely benign Candidiasis, familial, 6 2023-09-24 criteria provided, single submitter clinical testing

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