ClinVar Miner

Submissions for variant NM_001365536.1(SCN9A):c.2104+7A>G

dbSNP: rs886042850
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000403977 SCV000336955 uncertain significance not provided 2015-11-06 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005213252 SCV005851804 likely benign Neuropathy, hereditary sensory and autonomic, type 2A; Generalized epilepsy with febrile seizures plus, type 7 2024-05-21 criteria provided, single submitter clinical testing

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