ClinVar Miner

Submissions for variant NM_001040108.2(MLH3):c.3828-15A>C

gnomAD frequency: 0.00005  dbSNP: rs200169541
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 RCV000583210 SCV002760748 likely benign not specified 2025-03-04 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV000583210 SCV000691873 likely benign not specified no assertion criteria provided clinical testing

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