ClinVar Miner

Submissions for variant NM_000334.4(SCN4A):c.768C>G (p.Leu256=)

dbSNP: rs1597985505
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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 RCV000914198 SCV001059363 likely benign Hyperkalemic periodic paralysis 2019-07-30 criteria provided, single submitter clinical testing

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