ClinVar Miner

Submissions for variant NM_001001344.3(ATP2B3):c.2839+33A>G

gnomAD frequency: 0.99672  dbSNP: rs2980018
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001553936 SCV001775045 benign X-linked progressive cerebellar ataxia 2021-07-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004714282 SCV005274881 benign not provided criteria provided, single submitter not provided

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