ClinVar Miner

Submissions for variant NM_000535.6(PMS2):c.-93G>T

dbSNP: rs6976537
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000319974 SCV000484309 likely benign Lynch syndrome 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001675891 SCV001892770 benign not provided 2015-03-03 criteria provided, single submitter clinical testing

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