ClinVar Miner

Submissions for variant NM_153460.4(IL17RC):c.952G>A (p.Ala318Thr)

gnomAD frequency: 0.00366  dbSNP: rs145516404
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000885068 SCV001028494 benign Candidiasis, familial, 9 2024-01-25 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV001824902 SCV004699379 benign not provided 2024-02-01 criteria provided, single submitter clinical testing IL17RC: BP4, BS1, BS2
GenomeConnect, ClinGen RCV001824902 SCV002074662 not provided not provided no assertion provided phenotyping only Variant interpreted as Benign and reported on 04-27-2020 by Lab or GTR ID 500031. GenomeConnect assertions are reported exactly as they appear on the patient-provided report from the testing laboratory. GenomeConnect staff make no attempt to reinterpret the clinical significance of the variant. This variant was reported in an individual referred for clinical diagnostic genetic testing.

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