ClinVar Miner

List of variants in gene WWOX reported as pathogenic for Autosomal recessive spinocerebellar ataxia 12; Developmental and epileptic encephalopathy, 28

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_016373.4(WWOX):c.172+1G>C	rs1377640182	0.00001
NM_016373.4(WWOX):c.107+1G>A	rs1300924648

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