ClinVar Miner

List of variants in gene RAG1 reported as pathogenic by Illumina Laboratory Services, Illumina

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)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000448.3(RAG1):c.256_257del (p.Lys86fs)	rs772962160	0.00005
NM_000448.3(RAG1):c.322C>T (p.Arg108Ter)	rs193922464	0.00003

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