ClinVar Miner

Submissions for variant NM_001127222.2(CACNA1A):c.72C>T (p.Val24=)

dbSNP: rs773531250
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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 RCV001727075 SCV001961784 likely benign not provided 2021-07-01 criteria provided, single submitter clinical testing

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