ClinVar Miner

Submissions for variant NM_000546.6(TP53):c.559+24C>T

gnomAD frequency: 0.00008  dbSNP: rs56181208
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV000581705 SCV002551058 benign not specified 2025-03-04 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV000581705 SCV000692081 benign not specified no assertion criteria provided clinical testing

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