ClinVar Miner

Submissions for variant NM_018896.5(CACNA1G):c.3111G>A (p.Pro1037=)

gnomAD frequency: 0.00125  dbSNP: rs201745304
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000890372 SCV001034114 benign not provided 2024-01-22 criteria provided, single submitter clinical testing
GeneDx RCV000890372 SCV001856154 benign not provided 2021-04-23 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000890372 SCV004145647 likely benign not provided 2024-03-01 criteria provided, single submitter clinical testing CACNA1G: BP4, BP7, BS1

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