List of variants in gene RNF168 reported as likely pathogenic for not provided

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_152617.4(RNF168):c.391C>T (p.Arg131Ter)	rs201915239	0.00001
NM_152617.4(RNF168):c.493C>T (p.Arg165Ter)	rs148275050	0.00001
NM_152617.4(RNF168):c.1323_1326del (p.Gln442fs)	rs1047608955
NM_152617.4(RNF168):c.558+1G>A
NM_152617.4(RNF168):c.558+1G>T
NM_152617.4(RNF168):c.559-1_560del

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