ClinVar Miner

Submissions for variant NM_000334.4(SCN4A):c.3357C>T (p.Tyr1119=)

dbSNP: rs903219930
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000553102 SCV000658556 likely benign Hyperkalemic periodic paralysis 2022-04-21 criteria provided, single submitter clinical testing

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