List of variants in gene RAG1 reported as uncertain significance 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000448.3(RAG1):c.*834dup	rs745747958	0.00063
NM_000448.3(RAG1):c.1A>G (p.Met1Val)	rs200575481	0.00007
NM_000448.3(RAG1):c.*3122del	rs141384582
NM_000448.3(RAG1):c.*386del	rs886048258
NM_000448.3(RAG1):c.*856C>A	rs886048261

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