ClinVar Miner

Submissions for variant NM_000702.4(ATP1A2):c.681C>T (p.Pro227=)

gnomAD frequency: 0.00001  dbSNP: rs771930383
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 RCV002220113 SCV002363831 likely benign Familial hemiplegic migraine 2023-07-15 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003403680 SCV004122734 likely benign not specified 2023-10-11 criteria provided, single submitter clinical testing

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