List of variants in gene RAG1 reported as likely pathogenic by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000448.3(RAG1):c.1566G>T (p.Trp522Cys)	rs193922461	0.00009
NM_000448.3(RAG1):c.2603C>T (p.Ala868Val)	rs193922462	0.00007
NM_000448.3(RAG1):c.1303A>G (p.Met435Val)	rs141524540	0.00003
NM_000448.3(RAG1):c.2189G>T (p.Cys730Phe)	rs770771227	0.00003
NM_000448.3(RAG1):c.322C>T (p.Arg108Ter)	rs193922464	0.00003
NM_000448.3(RAG1):c.2345T>A (p.Val782Asp)	rs200300629	0.00001
NM_000448.3(RAG1):c.1438A>G (p.Ser480Gly)	rs772340017
NM_000448.3(RAG1):c.2904C>A (p.Asn968Lys)	rs193922463

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