List of variants in gene RAG2 reported as benign for Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000536.4(RAG2):c.*328A>G	rs10836573	0.48132
NM_000536.4(RAG2):c.878A>G (p.Glu293Gly)	rs16929093	0.03307
NM_000536.4(RAG2):c.*183C>A	rs12280564	0.03300
NM_000536.4(RAG2):c.*144G>T	rs12280515	0.03006
NM_000536.4(RAG2):c.741G>A (p.Val247=)	rs34092949	0.01926
NM_000536.4(RAG2):c.1158C>A (p.Phe386Leu)	rs34629171	0.01070
NM_000536.4(RAG2):c.644C>T (p.Thr215Ile)	rs35691292	0.00032

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