ClinVar Miner

Submissions for variant NM_002294.3(LAMP2):c.184-7C>G

dbSNP: rs397516737
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000037409 SCV000061066 uncertain significance not specified 2010-06-25 criteria provided, single submitter clinical testing Variant classified as Uncertain Significance - Favor Pathogenic.

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