ClinVar Miner

Submissions for variant NM_001165963.4(SCN1A):c.3426A>G (p.Lys1142=)

gnomAD frequency: 0.00001  dbSNP: rs753202524
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV000585996 SCV000697764 likely benign not specified 2019-08-29 criteria provided, single submitter clinical testing

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