ClinVar Miner

Submissions for variant NM_153460.4(IL17RC):c.970G>A (p.Ala324Thr)

gnomAD frequency: 0.01170  dbSNP: rs115461448
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 RCV000530442 SCV000656224 benign Candidiasis, familial, 9 2024-01-31 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004708952 SCV005238673 benign not provided criteria provided, single submitter not provided

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