ClinVar Miner

Submissions for variant NM_000702.4(ATP1A2):c.2622T>C (p.Gly874=)

dbSNP: rs886043454
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000260299 SCV000340253 uncertain significance not provided 2016-03-25 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001396923 SCV001598661 likely benign Familial hemiplegic migraine 2023-10-03 criteria provided, single submitter clinical testing

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