List of variants in gene RAG1 reported as benign 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: 16

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HGVS	dbSNP	gnomAD frequency
NM_000448.3(RAG1):c.746A>G (p.His249Arg)	rs3740955	0.48330
NM_000448.3(RAG1):c.*3184G>A	rs1056403	0.48229
NM_000448.3(RAG1):c.2459A>G (p.Lys820Arg)	rs2227973	0.12928
NM_000448.3(RAG1):c.-65A>G	rs872053	0.07575
NM_000448.3(RAG1):c.*2246T>C	rs4151045	0.07480
NM_000448.3(RAG1):c.2880A>G (p.Ala960=)	rs1980131	0.07459
NM_000448.3(RAG1):c.*1083C>T	rs4151040	0.06163
NM_000448.3(RAG1):c.906C>A (p.Asp302Glu)	rs4151030	0.02153
NM_000448.3(RAG1):c.303G>A (p.Ala101=)	rs4151025	0.01561
NM_000448.3(RAG1):c.189A>G (p.Pro63=)	rs34357808	0.01436
NM_000448.3(RAG1):c.2638G>A (p.Glu880Lys)	rs4151033	0.01395
NM_000448.3(RAG1):c.1346G>A (p.Arg449Lys)	rs4151031	0.01002
NM_000448.3(RAG1):c.251A>G (p.His84Arg)	rs150199231	0.00508
NM_000448.3(RAG1):c.2659G>A (p.Asp887Asn)	rs4151034	0.00364
NM_000448.3(RAG1):c.577G>A (p.Glu193Lys)	rs34841221	0.00204
NM_000448.3(RAG1):c.1573C>T (p.Pro525Ser)	rs4151032	0.00070

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