ClinVar Miner

Submissions for variant NM_002185.5(IL7R):c.537+4T>C

gnomAD frequency: 0.00002  dbSNP: rs200625485
Minimum review status: Collection method:
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001517811 SCV001726387 benign Immunodeficiency 104 2023-08-14 criteria provided, single submitter clinical testing

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