List of variants in gene RAG2 reported as likely benign for lymphoid system disorder

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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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000536.4(RAG2):c.1158C>A (p.Phe386Leu)	rs34629171	0.01070
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.477C>T (p.Arg159=)	rs141659100	0.00037
NM_000536.4(RAG2):c.1443T>C (p.His481=)	rs560115611	0.00004
NM_000536.4(RAG2):c.63G>A (p.Leu21=)	rs142797325	0.00001
NM_000536.4(RAG2):c.1391G>A (p.Arg464His)	rs147748696

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