ClinVar Miner

Submissions for variant NM_001127222.2(CACNA1A):c.7369G>T (p.Ala2457Ser)

dbSNP: rs954720308
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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 RCV001531290 SCV001746319 uncertain significance not provided 2021-05-01 criteria provided, single submitter clinical testing

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