ClinVar Miner

Submissions for variant NM_001145252.3(CFP):c.403+9G>A

gnomAD frequency: 0.00217  dbSNP: rs8177075
Minimum review status: Collection method:
Minimum conflict level:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV006457292 SCV007343339 likely benign not specified 2026-01-22 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001517135 SCV001725571 benign not provided 2025-12-11 criteria provided, single submitter clinical testing

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