Variant: rs1564995611 

    present in Gene: RAG1;IFTAP;RAG2
    present in Chromosome: 11
    Position on Chromosome: 36592803
    Alleles of this Variant: C/T

rs1564995611 in RAG1;IFTAP;RAG2 gene and Omenn Syndrome PMID 19470080 2009 Omenn syndrome due to mutation of the RAG2 gene.

rs1564995611 in RAG1;IFTAP;RAG2 gene and Primary immune deficiency disorder PMID 19470080 2009 Omenn syndrome due to mutation of the RAG2 gene.