ClinVar Miner

Submissions for variant NM_001127222.2(CACNA1A):c.3644A>G (p.Lys1215Arg)

dbSNP: rs1425955042
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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 RCV002214095 SCV002498435 uncertain significance not provided 2022-02-01 criteria provided, single submitter clinical testing

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