ClinVar Miner

Submissions for variant NM_000702.4(ATP1A2):c.1866G>A (p.Lys622=)

gnomAD frequency: 0.00001  dbSNP: rs763242526
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001466267 SCV001670269 likely benign Familial hemiplegic migraine 2018-02-06 criteria provided, single submitter clinical testing

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