ClinVar Miner

Submissions for variant NM_000702.4(ATP1A2):c.2181T>C (p.Ile727=)

gnomAD frequency: 0.00003  dbSNP: rs764960268
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 RCV001421043 SCV001623557 likely benign Familial hemiplegic migraine 2024-08-12 criteria provided, single submitter clinical testing

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