ClinVar Miner

Submissions for variant NM_153460.4(IL17RC):c.1680G>A (p.Val560=)

gnomAD frequency: 0.00109  dbSNP: rs144732629
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 RCV000974052 SCV001121861 benign Candidiasis, familial, 9 2024-01-20 criteria provided, single submitter clinical testing

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