List of variants in gene RAG2 reported by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 17

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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.1504A>G (p.Met502Val)	rs145614809	0.00149
NM_000536.4(RAG2):c.477C>T (p.Arg159=)	rs141659100	0.00037
NM_000536.4(RAG2):c.644C>T (p.Thr215Ile)	rs35691292	0.00032
NM_000536.4(RAG2):c.1352G>C (p.Gly451Ala)	rs121918575	0.00004
NM_000536.4(RAG2):c.217C>T (p.Arg73Cys)	rs193922574	0.00003
NM_000536.4(RAG2):c.283G>A (p.Gly95Arg)	rs36001797	0.00003
NM_000536.4(RAG2):c.1006A>G (p.Lys336Glu)	rs1490516072	0.00001
NM_000536.4(RAG2):c.1309G>A (p.Glu437Lys)	rs193922573	0.00001
NM_000536.4(RAG2):c.328A>C (p.Met110Leu)	rs193922575	0.00001
NM_000536.4(RAG2):c.104G>C (p.Gly35Ala)	rs148508754
NM_000536.4(RAG2):c.1247G>T (p.Trp416Leu)	rs193922572
NM_000536.4(RAG2):c.1295C>T (p.Pro432Leu)	rs753677011
NM_000536.4(RAG2):c.193G>T (p.Asp65Tyr)	rs909264507
NM_000536.4(RAG2):c.353A>G (p.Lys118Arg)	rs1851094033
NM_000536.4(RAG2):c.501A>C (p.Arg167Ser)	rs1159686210
NM_000536.4(RAG2):c.95G>A (p.Gly32Glu)

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