ClinVar Miner

Submissions for variant NM_000702.4(ATP1A2):c.1652-8C>T

gnomAD frequency: 0.00022  dbSNP: rs370023134
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000733204 SCV000521734 likely benign not provided 2019-01-08 criteria provided, single submitter clinical testing
Eurofins Ntd Llc (ga) RCV000733204 SCV000861239 uncertain significance not provided 2018-05-29 criteria provided, single submitter clinical testing
Invitae RCV001079040 SCV001009203 likely benign Familial hemiplegic migraine 2023-11-08 criteria provided, single submitter clinical testing

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