List of variants in gene RAG1 reported as likely pathogenic for Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive

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
NM_000448.3(RAG1):c.1073G>A (p.Cys358Tyr)
NM_000448.3(RAG1):c.1219C>G (p.Gln407Glu)	rs986694616
NM_000448.3(RAG1):c.1767C>G (p.Tyr589Ter)	rs991089005
NM_000448.3(RAG1):c.2393A>G (p.His798Arg)	rs2133297434

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