ClinVar Miner

Submissions for variant NM_014339.7(IL17RA):c.944-5C>T

gnomAD frequency: 0.00002  dbSNP: rs370875549
Minimum review status: Collection method:
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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 RCV000920138 SCV001065498 likely benign Immunodeficiency 51 2024-10-17 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV000920138 SCV002806071 likely benign Immunodeficiency 51 2021-10-21 criteria provided, single submitter clinical testing

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