ClinVar Miner

Submissions for variant NM_006514.4(SCN10A):c.2106+8C>T

gnomAD frequency: 0.00027  dbSNP: rs368212766
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000638789 SCV000760338 likely benign Brugada syndrome 2024-09-17 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002507084 SCV002807326 likely benign Episodic pain syndrome, familial, 2 2021-10-14 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV001700283 SCV001921342 likely benign not provided no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001700283 SCV001959210 likely benign not provided no assertion criteria provided clinical testing

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