ClinVar Miner

Submissions for variant NM_002294.3(LAMP2):c.1134C>T (p.Pro378=)

dbSNP: rs2147273218
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001394721 SCV001596411 likely benign Danon disease 2022-07-18 criteria provided, single submitter clinical testing

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