RS1064793251 RAG2

Health Risk Chr 11:36593630
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What This Variant Does
"CLNSIG=4
Associated Conditions
Atypical severe combined immunodeficiency due to complete RAG1/2 deficiency
Recombinase activating gene 2 deficiency
Inborn error of immunity
Atypical severe combined immunodeficiency due to complete RAG1/2 deficiency
Recombinase activating gene 2 deficiency
Inborn error of immunity
Other Variants in RAG2
rs121918573 rs121917894 rs121917895 rs121917896 rs36001797 rs2133313409 rs121917897 rs121918574 rs121918575 rs148508754
Ask Dr. Hemsworth about this variant