ClinVar Miner

Submissions for variant NM_001127222.2(CACNA1A):c.4556A>G (p.Lys1519Arg)

dbSNP: rs752888622
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV000996786 SCV001151707 uncertain significance not provided 2016-05-01 criteria provided, single submitter clinical testing

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