ClinVar Miner

Submissions for variant NM_014339.7(IL17RA):c.931+7del

dbSNP: rs531944007
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 RCV000536725 SCV000656923 benign Immunodeficiency 51 2023-12-12 criteria provided, single submitter clinical testing

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