List of variants in gene RAG1 reported as likely benign for Severe combined immunodeficiency disease

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NC_000011.10:g.36579767A>G	rs2673017	0.02522
NM_000448.3(RAG1):c.189A>G (p.Pro63=)	rs34357808	0.01436
NM_000448.3(RAG1):c.*2705dup	rs4151048
NM_000448.3(RAG1):c.*2936TAAG[1]	rs199555129

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