ClinVar Miner

Submissions for variant NM_001550.4(IFRD1):c.568-10T>A

gnomAD frequency: 0.00121  dbSNP: rs565300368
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Breakthrough Genomics, Breakthrough Genomics RCV001703335 SCV005221482 likely benign not provided criteria provided, single submitter not provided
Clinical Genetics, Academic Medical Center RCV001699685 SCV001924982 benign not specified no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001703335 SCV001928601 likely benign not provided no assertion criteria provided clinical testing

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