RS121917897 RAG2
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What This Variant Does
"CLNSIG=5
Associated Conditions
Severe combined immunodeficiency
B cell-negative
Histiocytic medullary reticulosis
autosomal recessive
T cell-negative
NK cell-positive
Recombinase activating gene 2 deficiency
Inborn error of immunity
Severe combined immunodeficiency
B cell-negative
Histiocytic medullary reticulosis
autosomal recessive
T cell-negative
NK cell-positive
Recombinase activating gene 2 deficiency
Other Variants in RAG2