ClinVar Miner

Submissions for variant NM_002294.3(LAMP2):c.*3459GTT[3]

dbSNP: rs199705754
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000288949 SCV000481523 likely benign Danon disease 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000327789 SCV000481524 likely benign Hypertrophic cardiomyopathy 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001785606 SCV002028078 likely benign not provided 2021-05-20 criteria provided, single submitter clinical testing

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