ClinVar Miner

Submissions for variant NM_000702.4(ATP1A2):c.627T>C (p.Cys209=) (rs139229302)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000336764 SCV000349882 uncertain significance Familial hemiplegic migraine 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000407917 SCV000349883 uncertain significance Alternating hemiplegia of childhood 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000859054 SCV000556866 likely benign not provided 2016-09-11 criteria provided, single submitter clinical testing

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