ClinVar Miner

Submissions for variant NM_000702.4(ATP1A2):c.2284+62T>A

dbSNP: rs1651915554
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Cell and Molecular Biology Laboratory, University of the Punjab Lahore RCV001270448 SCV001450521 likely benign Seizures, benign familial infantile, 3 no assertion criteria provided case-control

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