List of variants in gene WDR73 reported as likely benign for autosomal recessive congenital cerebellar ataxia

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_032856.5(WDR73):c.336G>A (p.Gln112=)	rs73449331	0.00970
NM_032856.5(WDR73):c.41+262G>A	rs147776100	0.00888
NM_032856.5(WDR73):c.883+8C>T	rs200133030	0.00072
NM_032856.5(WDR73):c.354T>G (p.Asp118Glu)	rs201827208	0.00016
NM_032856.5(WDR73):c.33C>T (p.Ser11=)	rs376620550	0.00010
NM_032856.5(WDR73):c.267A>G (p.Leu89=)	rs772299478	0.00006
NM_032856.5(WDR73):c.816T>C (p.Pro272=)	rs374742538	0.00001

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