ClinVar Miner

List of variants in gene RAG1 reported as likely pathogenic for RAG1-related disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000448.3(RAG1):c.2488A>T (p.Lys830Ter)	rs755551812	0.00002
NM_000448.3(RAG1):c.2327G>A (p.Arg776Gln)	rs1254739284	0.00001

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