List of variants in gene RNF168 reported as benign for RIDDLE syndrome

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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: 9

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HGVS	dbSNP	gnomAD frequency
NM_152617.4(RNF168):c.559-46A>G	rs7646174	0.58484
NM_152617.4(RNF168):c.1202C>A (p.Pro401Gln)	rs3796129	0.49737
NM_152617.4(RNF168):c.972G>A (p.Glu324=)	rs35405598	0.02354
NM_152617.4(RNF168):c.307G>A (p.Asp103Asn)	rs149773824	0.01095
NM_152617.4(RNF168):c.1481C>T (p.Pro494Leu)	rs35132476	0.00738
NM_152617.4(RNF168):c.1284A>G (p.Lys428=)	rs78211871	0.00550
NM_152617.4(RNF168):c.1237G>A (p.Glu413Lys)	rs6790173	0.00395
NM_152617.4(RNF168):c.508G>A (p.Glu170Lys)	rs114025031	0.00235
NM_152617.4(RNF168):c.378+26del	rs62798260

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