ClinVar Miner

Submissions for variant NM_000334.4(SCN4A):c.704-6G>C

dbSNP: rs368225907
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002109220 SCV002432513 likely benign Familial hyperkalemic periodic paralysis 2021-05-03 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003426345 SCV004138808 likely benign not provided 2022-06-01 criteria provided, single submitter clinical testing SCN4A: BP4

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