ClinVar Miner

Submissions for variant NC_000002.12:g.(?_166227650)_(166227743_?)del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000533008 SCV000649259 uncertain significance Neuropathy, hereditary sensory and autonomic, type 2A; Generalized epilepsy with febrile seizures plus, type 7 2017-07-29 criteria provided, single submitter clinical testing This variant is an in-frame deletion of the genomic region encompassing exon 23 of the SCN9A gene. It preserves the integrity of the reading frame. This variant has not been reported in the literature in individuals with SCN9A-related disease. Experimental studies and prediction algorithms are not available for this variant, and the functional significance of the deleted amino acids is currently unknown. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.

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