ClinVar Miner

Submissions for variant NM_001040108.1(MLH3):c.2167G>A (p.Val723Ile) (rs28756989)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000344792 SCV000388777 uncertain significance Lynch syndrome 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000474795 SCV000562040 benign MLH3-Related Lynch Syndrome 2017-12-01 criteria provided, single submitter clinical testing

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