ClinVar Miner

Submissions for variant NM_000249.3(MLH1):c.589-9G>A (rs566497442)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000226353 SCV000284068 likely benign Lynch syndrome 2016-03-28 criteria provided, single submitter clinical testing
Color RCV000579461 SCV000684849 likely benign Hereditary cancer-predisposing syndrome 2016-06-06 criteria provided, single submitter clinical testing

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