Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1564995611
rs1564995611
RAG1 ; RAG2 ; IFTAP
T 0.700 GeneticVariation CLINVAR Omenn syndrome due to mutation of the RAG2 gene. 19470080

2009