Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs150739647
rs150739647
RAG1 ; RAG2
A 0.700 CausalMutation CLINVAR Rapid molecular diagnostics of severe primary immunodeficiency determined by using targeted next-generation sequencing. 27484032

2016
dbSNP: rs150739647
rs150739647
RAG1 ; RAG2
A 0.700 CausalMutation CLINVAR Mutations in Recombination Activating Gene 1 and 2 in patients with severe combined immunodeficiency disorders in Egypt. 25869295

2015
dbSNP: rs150739647
rs150739647
RAG1 ; RAG2
A 0.700 CausalMutation CLINVAR Highly variable clinical phenotypes of hypomorphic RAG1 mutations. 20956421

2010
dbSNP: rs150739647
rs150739647
RAG1 ; RAG2
A 0.700 CausalMutation CLINVAR An immunodeficiency disease with RAG mutations and granulomas. 18463379

2008
dbSNP: rs150739647
rs150739647
RAG1 ; RAG2
A 0.700 CausalMutation CLINVAR A RAG1 mutation found in Omenn syndrome causes coding flank hypersensitivity: a novel mechanism for antigen receptor repertoire restriction. 18768869

2008
dbSNP: rs150739647
rs150739647
RAG1 ; RAG2
A 0.700 CausalMutation CLINVAR GvHD-associated cytokine polymorphisms do not associate with Omenn syndrome rather than T-B- SCID in patients with defects in RAG genes. 17572155

2007
dbSNP: rs150739647
rs150739647
RAG1 ; RAG2
A 0.700 CausalMutation CLINVAR Mutational analysis of all conserved basic amino acids in RAG-1 reveals catalytic, step arrest, and joining-deficient mutants in the V(D)J recombinase. 11971977

2002
dbSNP: rs150739647
rs150739647
RAG1 ; RAG2
A 0.700 CausalMutation CLINVAR The genetic and biochemical basis of Omenn syndrome. 11213808

2000