RS121918575 RAG2
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What This Variant Does
"[OMIM:?]
Associated Conditions
Combined immunodeficiency with skin granulomas
Inborn error of immunity
Recombinase activating gene 2 deficiency
Severe combined immunodeficiency
autosomal recessive
T cell-negative
B cell-negative
NK cell-positive
Common variable immunodeficiency
Severe combined immunodeficiency disease
Histiocytic medullary reticulosis
Combined immunodeficiency with skin granulomas
Inborn error of immunity
Recombinase activating gene 2 deficiency
Severe combined immunodeficiency
Other Variants in RAG2