RS121917896 RAG2

Health Risk Chr 11:36593315
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What This Variant Does
"CLNSIG=5
Associated Conditions
Histiocytic medullary reticulosis
Recombinase activating gene 2 deficiency
Inborn error of immunity
Severe combined immunodeficiency disease
Histiocytic medullary reticulosis
Recombinase activating gene 2 deficiency
Inborn error of immunity
Severe combined immunodeficiency disease
Other Variants in RAG2
rs121918573 rs121917894 rs121917895 rs36001797 rs2133313409 rs121917897 rs121918574 rs121918575 rs148508754 rs193922572
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