List of variants in gene RNF168 reported as likely pathogenic for 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_152617.4(RNF168):c.493C>T (p.Arg165Ter)	rs148275050	0.00001
NM_152617.4(RNF168):c.559-1_560del
NM_152617.4(RNF168):c.659_662del (p.Arg220fs)	rs755314562

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