ClinVar Miner

Submissions for variant NM_000702.4(ATP1A2):c.2620G>A (p.Gly874Ser)

dbSNP: rs1651959213
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV001200370 SCV001371310 likely pathogenic not provided 2020-08-01 criteria provided, single submitter clinical testing
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre RCV003989128 SCV004805851 uncertain significance Migraine, familial hemiplegic, 2 2024-03-29 criteria provided, single submitter clinical testing

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