List of variants in gene RAG2 reported as likely 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000536.4(RAG2):c.*227T>C	rs113343318	0.00331
NM_000536.4(RAG2):c.22G>A (p.Val8Ile)	rs150762709	0.00313
NM_000536.4(RAG2):c.1095T>C (p.Ser365=)	rs140519815	0.00139
NM_000536.4(RAG2):c.*52T>A	rs546979744	0.00076
NM_000536.4(RAG2):c.644C>T (p.Thr215Ile)	rs35691292	0.00032

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