ClinVar Miner

Submissions for variant NM_000249.4(MLH1):c.55_63delinsT (p.Ile19fs)

dbSNP: rs2125694105
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
University of Science and Technology Houari Boumediene, Laboratory of Molecular and Cellular Biology (LBCM) RCV001849899 SCV002106382 pathogenic Lynch syndrome 1 2024-04-04 criteria provided, single submitter clinical testing

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