ClinVar Miner

Submissions for variant NM_000702.4(ATP1A2):c.1155C>T (p.Thr385=)

gnomAD frequency: 0.00001  dbSNP: rs759207376
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 RCV001434565 SCV001637375 likely benign Familial hemiplegic migraine 2024-07-11 criteria provided, single submitter clinical testing

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