ClinVar Miner

Submissions for variant NM_006060.6(IKZF1):c.99C>A (p.Ile33=)

gnomAD frequency: 0.00491  dbSNP: rs61732861
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV001819261 SCV002067223 benign not specified 2021-10-20 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002542555 SCV003011144 benign not provided 2025-01-23 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV002542555 SCV005227348 likely benign not provided criteria provided, single submitter not provided

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