Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894287
rs104894287
RAG1 ; RAG2
0.800 GeneticVariation UNIPROT A novel immunodeficiency associated with hypomorphic RAG1 mutations and CMV infection. 16276422

2005
dbSNP: rs104894288
rs104894288
RAG1 ; RAG2
0.800 GeneticVariation UNIPROT A novel immunodeficiency associated with hypomorphic RAG1 mutations and CMV infection. 16276422

2005
dbSNP: rs104894287
rs104894287
RAG1 ; RAG2
T 0.800 CausalMutation CLINVAR

dbSNP: rs104894288
rs104894288
RAG1 ; RAG2
C 0.800 CausalMutation CLINVAR

dbSNP: rs141524540
rs141524540
RAG1
G 0.700 GeneticVariation CLINVAR

dbSNP: rs754502950
rs754502950
RAG1 ; RAG2
G 0.700 GeneticVariation CLINVAR

dbSNP: rs773929270
rs773929270
RAG1
T 0.700 CausalMutation CLINVAR