ClinVar Miner

Submissions for variant NM_002294.3(LAMP2):c.*2148AT[8]

dbSNP: rs753399289
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000392846 SCV000481551 uncertain significance Hypertrophic cardiomyopathy 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000305072 SCV000481552 uncertain significance Danon disease 2016-06-14 criteria provided, single submitter clinical testing

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