RS121908735 ADA
Upload your DNA to see your genotype for this variant.
What This Variant Does
"Identification of two new missense mutations (R156C and S291L) in two ADA- SCID patients unusual for...
Associated Conditions
Severe combined immunodeficiency
autosomal recessive
T cell-negative
B cell-negative
NK cell-negative
due to adenosine deaminase deficiency
Severe combined immunodeficiency disease
Severe combined immunodeficiency disease
Severe combined immunodeficiency
autosomal recessive
T cell-negative
B cell-negative
NK cell-negative
due to adenosine deaminase deficiency
Severe combined immunodeficiency disease
Other Variants in ADA