ClinVar Miner

Submissions for variant NM_000702.4(ATP1A2):c.2123T>C (p.Ile708Thr)

gnomAD frequency: 0.00001  dbSNP: rs1341609289
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 RCV001216193 SCV001387975 uncertain significance Familial hemiplegic migraine 2021-08-27 criteria provided, single submitter clinical testing
Athena Diagnostics RCV001664759 SCV001880093 uncertain significance not provided 2021-06-08 criteria provided, single submitter clinical testing

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