ClinVar Miner

Submissions for variant NM_000249.4(MLH1):c.976G>T (p.Val326Leu)

dbSNP: rs730881739
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomics Laboratory, Virgen de la Arrixaca University Clinical Hospital RCV001580775 SCV001810157 uncertain significance Hereditary breast ovarian cancer syndrome criteria provided, single submitter clinical testing
Baylor Genetics RCV003470869 SCV004192991 uncertain significance Colorectal cancer, hereditary nonpolyposis, type 2 2023-06-06 criteria provided, single submitter clinical testing

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