ClinVar Miner

Submissions for variant NM_000249.4(MLH1):c.1039-25T>A

gnomAD frequency: 0.00064  dbSNP: rs764852270
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV000584341 SCV002552486 likely benign not specified 2025-03-04 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004711200 SCV005258446 likely benign not provided criteria provided, single submitter not provided
Mayo Clinic Laboratories, Mayo Clinic RCV000584341 SCV000691857 likely benign not specified no assertion criteria provided clinical testing

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