ClinVar Miner

Submissions for variant NM_001040108.2(MLH3):c.3570+28A>T

gnomAD frequency: 0.00949  dbSNP: rs67547819
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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 RCV000584520 SCV002551407 benign not specified 2023-08-15 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV000584520 SCV000691877 likely benign not specified no assertion criteria provided clinical testing

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