ClinVar Miner

Submissions for variant NM_000900.5(MGP):c.62-18dup

dbSNP: rs11393307
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000293303 SCV000377157 benign Keutel syndrome 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001512346 SCV001719744 benign not provided 2024-01-31 criteria provided, single submitter clinical testing
GeneDx RCV001512346 SCV001751953 benign not provided 2018-11-09 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003977896 SCV004798279 benign MGP-related disorder 2019-05-24 no assertion criteria provided clinical testing This variant is classified as benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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