List of variants in gene combination IFTAP, RAG2 reported as uncertain significance for immune system 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)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000536.4(RAG2):c.-151A>C	rs886048273	0.00003
NM_000536.4(RAG2):c.-146G>T	rs1851360292

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