ClinVar Miner

Submissions for variant NM_000702.4(ATP1A2):c.1779G>A (p.Arg593=)

dbSNP: rs1553245179
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000635229 SCV000756613 likely benign Familial hemiplegic migraine 2019-12-31 criteria provided, single submitter clinical testing
GeneDx RCV001584465 SCV001812820 likely benign not provided 2021-06-15 criteria provided, single submitter clinical testing

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