ClinVar Miner

Submissions for variant NM_000702.4(ATP1A2):c.909C>T (p.Ser303=)

dbSNP: rs1422290691
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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) RCV000593347 SCV000707179 uncertain significance not provided 2017-04-17 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002531074 SCV003514898 likely benign Familial hemiplegic migraine 2022-08-31 criteria provided, single submitter clinical testing

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