ClinVar Miner

Submissions for variant NM_153460.4(IL17RC):c.591C>T (p.Leu197=)

gnomAD frequency: 0.00223  dbSNP: rs139727834
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 RCV000652973 SCV000774846 benign Candidiasis, familial, 9 2024-01-31 criteria provided, single submitter clinical testing

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