ClinVar Miner

Submissions for variant NM_000702.4(ATP1A2):c.1083G>A (p.Ala361=)

gnomAD frequency: 0.00001  dbSNP: rs778171140
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001483230 SCV001687615 likely benign Familial hemiplegic migraine 2025-01-30 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004711676 SCV005264264 likely benign not provided criteria provided, single submitter not provided

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