Gene: RAG1 ×
Source: UNIPROT ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894284
rs104894284
RAG1
0.810 GeneticVariation UNIPROT Novel mutations in RAG1/2 and ADA genes in Israeli patients presenting with T-B-SCID or Omenn syndrome. 21624848

2011
dbSNP: rs104894284
rs104894284
RAG1
0.810 GeneticVariation UNIPROT Clinical characteristics and molecular analysis of three Chinese children with Omenn syndrome. 21771083

2011
dbSNP: rs104894284
rs104894284
RAG1
0.810 GeneticVariation UNIPROT Molecular analysis of T-B-NK+ severe combined immunodeficiency and Omenn syndrome cases in Saudi Arabia. 19912631

2009
dbSNP: rs104894284
rs104894284
RAG1
0.810 GeneticVariation UNIPROT V(D)J recombination defects in lymphocytes due to RAG mutations: severe immunodeficiency with a spectrum of clinical presentations. 11133745

2001
dbSNP: rs104894284
rs104894284
RAG1
0.810 GeneticVariation UNIPROT Characterization of immune function and analysis of RAG gene mutations in Omenn syndrome and related disorders. 10606976

2000
dbSNP: rs104894284
rs104894284
RAG1
0.810 GeneticVariation UNIPROT Partial V(D)J recombination activity leads to Omenn syndrome. 9630231

1998
dbSNP: rs104894285
rs104894285
RAG1
0.800 GeneticVariation UNIPROT Novel mutations in RAG1/2 and ADA genes in Israeli patients presenting with T-B-SCID or Omenn syndrome. 21624848

2011
dbSNP: rs104894285
rs104894285
RAG1
0.800 GeneticVariation UNIPROT Clinical characteristics and molecular analysis of three Chinese children with Omenn syndrome. 21771083

2011
dbSNP: rs104894286
rs104894286
RAG1
0.800 GeneticVariation UNIPROT Novel mutations in RAG1/2 and ADA genes in Israeli patients presenting with T-B-SCID or Omenn syndrome. 21624848

2011
dbSNP: rs104894286
rs104894286
RAG1
0.800 GeneticVariation UNIPROT Clinical characteristics and molecular analysis of three Chinese children with Omenn syndrome. 21771083

2011
dbSNP: rs104894289
rs104894289
RAG1
0.800 GeneticVariation UNIPROT Novel mutations in RAG1/2 and ADA genes in Israeli patients presenting with T-B-SCID or Omenn syndrome. 21624848

2011
dbSNP: rs104894289
rs104894289
RAG1
0.800 GeneticVariation UNIPROT Clinical characteristics and molecular analysis of three Chinese children with Omenn syndrome. 21771083

2011
dbSNP: rs104894290
rs104894290
RAG1 ; RAG2
0.800 GeneticVariation UNIPROT Clinical characteristics and molecular analysis of three Chinese children with Omenn syndrome. 21771083

2011
dbSNP: rs104894290
rs104894290
RAG1 ; RAG2
0.800 GeneticVariation UNIPROT Novel mutations in RAG1/2 and ADA genes in Israeli patients presenting with T-B-SCID or Omenn syndrome. 21624848

2011
dbSNP: rs104894291
rs104894291
RAG1
0.800 GeneticVariation UNIPROT Clinical characteristics and molecular analysis of three Chinese children with Omenn syndrome. 21771083

2011
dbSNP: rs104894291
rs104894291
RAG1
0.800 GeneticVariation UNIPROT Novel mutations in RAG1/2 and ADA genes in Israeli patients presenting with T-B-SCID or Omenn syndrome. 21624848

2011
dbSNP: rs104894292
rs104894292
RAG1
0.800 GeneticVariation UNIPROT Clinical characteristics and molecular analysis of three Chinese children with Omenn syndrome. 21771083

2011
dbSNP: rs104894292
rs104894292
RAG1
0.800 GeneticVariation UNIPROT Novel mutations in RAG1/2 and ADA genes in Israeli patients presenting with T-B-SCID or Omenn syndrome. 21624848

2011
dbSNP: rs121918571
rs121918571
RAG1
0.800 GeneticVariation UNIPROT Novel mutations in RAG1/2 and ADA genes in Israeli patients presenting with T-B-SCID or Omenn syndrome. 21624848

2011
dbSNP: rs121918571
rs121918571
RAG1
0.800 GeneticVariation UNIPROT Clinical characteristics and molecular analysis of three Chinese children with Omenn syndrome. 21771083

2011
dbSNP: rs141524540
rs141524540
RAG1
0.800 GeneticVariation UNIPROT Novel mutations in RAG1/2 and ADA genes in Israeli patients presenting with T-B-SCID or Omenn syndrome. 21624848

2011
dbSNP: rs141524540
rs141524540
RAG1
0.800 GeneticVariation UNIPROT Clinical characteristics and molecular analysis of three Chinese children with Omenn syndrome. 21771083

2011
dbSNP: rs104894285
rs104894285
RAG1
0.800 GeneticVariation UNIPROT Molecular analysis of T-B-NK+ severe combined immunodeficiency and Omenn syndrome cases in Saudi Arabia. 19912631

2009
dbSNP: rs104894286
rs104894286
RAG1
0.800 GeneticVariation UNIPROT Molecular analysis of T-B-NK+ severe combined immunodeficiency and Omenn syndrome cases in Saudi Arabia. 19912631

2009
dbSNP: rs104894289
rs104894289
RAG1
0.800 GeneticVariation UNIPROT Molecular analysis of T-B-NK+ severe combined immunodeficiency and Omenn syndrome cases in Saudi Arabia. 19912631

2009