List of variants in gene WWOX reported as uncertain significance for Malignant tumor of esophagus; Autosomal recessive spinocerebellar ataxia 12; Developmental and epileptic encephalopathy, 28

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_016373.4(WWOX):c.935C>A (p.Ser312Tyr)	rs79399971	0.00038
NM_016373.4(WWOX):c.990C>G (p.Asn330Lys)	rs117209694	0.00016
NM_016373.4(WWOX):c.591C>G (p.Phe197Leu)	rs200847456	0.00011
NM_016373.4(WWOX):c.926G>A (p.Arg309His)	rs370792938	0.00004
NM_016373.4(WWOX):c.1039C>A (p.Pro347Thr)	rs200699154	0.00003
NM_016373.4(WWOX):c.746G>A (p.Arg249His)	rs756703833	0.00003
NM_016373.4(WWOX):c.517-108243C>T	rs551189075	0.00002
NM_016373.4(WWOX):c.59C>T (p.Pro20Leu)	rs761638116	0.00001
NM_016373.4(WWOX):c.341T>C (p.Met114Thr)	rs761906386
NM_016373.4(WWOX):c.535G>T (p.Ala179Ser)	rs11545029
NM_016373.4(WWOX):c.562C>A (p.Arg188Ser)	rs199511589

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