Variants in gene RAG2 with conflicting interpretations "likely pathogenic" and "pathogenic"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) method:
Gene type:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 8

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HGVS	dbSNP
NM_000536.4(RAG2):c.115A>G (p.Arg39Gly)	rs121917897
NM_000536.4(RAG2):c.123C>G (p.Cys41Trp)	rs121917895
NM_000536.4(RAG2):c.193G>T (p.Asp65Tyr)	rs909264507
NM_000536.4(RAG2):c.230C>A (p.Thr77Asn)	rs121918574
NM_000536.4(RAG2):c.283G>A (p.Gly95Arg)	rs36001797
NM_000536.4(RAG2):c.2T>C (p.Met1Thr)	rs1554947410
NM_000536.4(RAG2):c.539C>A (p.Pro180His)	rs1064793251
NM_000536.4(RAG2):c.854T>G (p.Met285Arg)	rs121917896

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