List of variants in gene RAG1 reported as uncertain significance by GeneDx

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000448.3(RAG1):c.725A>G (p.Gln242Arg)	rs76897604	0.00164
NM_000448.3(RAG1):c.1A>G (p.Met1Val)	rs200575481	0.00007
NM_000448.3(RAG1):c.335G>A (p.Arg112His)	rs749223640	0.00003
NM_000448.3(RAG1):c.1630C>A (p.Leu544Ile)	rs773829381	0.00001
NM_000448.3(RAG1):c.1875T>G (p.Phe625Leu)	rs749669514
NM_000448.3(RAG1):c.1988C>A (p.Ala663Glu)	rs2133296713
NM_000448.3(RAG1):c.506C>G (p.Ser169Trp)	rs4151027

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