ClinVar Miner

Submissions for variant NM_001127222.2(CACNA1A):c.1946del (p.Asn649fs)

dbSNP: rs1568518113
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
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 RCV000762260 SCV000892552 likely pathogenic not provided 2019-02-01 criteria provided, single submitter clinical testing

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