ClinVar Miner

List of variants in gene RAG2 reported as uncertain significance for RAG2-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_000536.4(RAG2):c.1198G>C (p.Asp400His)	rs140682926	0.00058
NM_000536.4(RAG2):c.809A>G (p.Glu270Gly)	rs149241274	0.00025

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