ClinVar Miner

Submissions for variant NM_001040108.1(MLH3):c.149T>A (p.Phe50Tyr) (rs148409389)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Centre for Mendelian Genomics,University Medical Centre Ljubljana RCV000415369 SCV000492820 uncertain significance Hereditary cancer 2014-05-20 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000382973 SCV000388792 uncertain significance Lynch syndrome 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000530139 SCV000659576 benign MLH3-Related Lynch Syndrome 2017-12-10 criteria provided, single submitter clinical testing

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