ClinVar Miner

Submissions for variant NM_000702.4(ATP1A2):c.*1630C>T

gnomAD frequency: 0.00001  dbSNP: rs886045433
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000322046 SCV000350016 uncertain significance Familial hemiplegic migraine 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000379004 SCV000350017 uncertain significance Alternating hemiplegia of childhood 2016-06-14 criteria provided, single submitter clinical testing

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