ClinVar Miner

Submissions for variant NM_000249.3(MLH1):c.588+8C>A (rs1060504005)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000461072 SCV000555991 likely benign Lynch syndrome 2016-12-24 criteria provided, single submitter clinical testing
Color RCV000773048 SCV000906443 likely benign Hereditary cancer-predisposing syndrome 2016-02-23 criteria provided, single submitter clinical testing

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