ClinVar Miner

Submissions for variant NM_000249.3(MLH1):c.-86G>A

dbSNP: rs558051715
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000342636 SCV000443322 uncertain significance Lynch syndrome 2016-06-14 criteria provided, single submitter clinical testing

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