ClinVar Miner

Submissions for variant NM_000249.3(MLH1):c.1039-8_1039-7insTA (rs535965616)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000160559 SCV000211138 benign Hereditary cancer-predisposing syndrome 2014-07-07 criteria provided, single submitter clinical testing The variant is found in HEREDICANCER,BR-OV-HEREDIC panel(s).
Invitae RCV000195736 SCV000253129 benign Hereditary nonpolyposis colorectal neoplasms 2019-12-11 criteria provided, single submitter clinical testing
Color RCV000160559 SCV001351740 likely benign Hereditary cancer-predisposing syndrome 2019-09-03 criteria provided, single submitter clinical testing

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