ClinVar Miner

Submissions for variant NM_001205293.3(CACNA1E):c.6905A>G (p.Asn2302Ser)

dbSNP: rs1662051174
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV001532088 SCV001747485 uncertain significance not provided 2021-06-01 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001532088 SCV004385836 benign not provided 2023-10-10 criteria provided, single submitter clinical testing

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