ClinVar Miner

Submissions for variant NM_016373.4(WWOX):c.107+252C>T

gnomAD frequency: 0.00633  dbSNP: rs58108921
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001547253 SCV001766911 likely benign not provided 2018-08-15 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002495874 SCV002800006 likely benign Malignant tumor of esophagus; Autosomal recessive spinocerebellar ataxia 12; Developmental and epileptic encephalopathy, 28 2021-10-08 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001547253 SCV005219199 likely benign not provided criteria provided, single submitter not provided

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