ClinVar Miner

Submissions for variant NM_001001331.4(ATP2B2):c.199+52G>A

gnomAD frequency: 0.03868  dbSNP: rs115504280
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001708229 SCV001935826 benign not provided 2021-05-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001708229 SCV005239284 benign not provided criteria provided, single submitter not provided

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