ClinVar Miner

Submissions for variant NM_001040108.2(MLH3):c.3570+29AT[10]

dbSNP: rs145063005
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001714408 SCV001945208 benign not provided 2019-08-15 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002279976 SCV002568049 likely benign not specified 2025-03-04 criteria provided, single submitter clinical testing

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