ClinVar Miner

List of variants in gene WWOX reported as uncertain significance for Autosomal recessive spinocerebellar ataxia 12

Minimum submission review status:		Collection method:
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.713A>G (p.Tyr238Cys)	rs142806268	0.00026
NM_016373.4(WWOX):c.517-108226G>T	rs1057518676

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