ClinVar Miner

Submissions for variant NM_001205293.3(CACNA1E):c.4647C>T (p.Thr1549=)

dbSNP: rs759613835
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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 RCV002217413 SCV002363261 likely benign not provided 2025-01-27 criteria provided, single submitter clinical testing

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