ClinVar Miner

Submissions for variant NM_052872.4(IL17F):c.222C>T (p.Ile74=)

gnomAD frequency: 0.00167  dbSNP: rs6931727
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 RCV000558026 SCV000650684 benign Candidiasis, familial, 6 2023-12-25 criteria provided, single submitter clinical testing

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