ClinVar Miner

Submissions for variant NM_001127222.2(CACNA1A):c.6964_6965insCAG (p.Gln2322delinsProGlu)

dbSNP: rs879255419
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Diagnostic Laboratory, Division of Genomic Diagnostics, Children's Hospital of Philadelphia RCV000239315 SCV000297309 benign not specified 2015-09-24 criteria provided, single submitter clinical testing

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