RS77563738 ADA2

Health Risk Chr 22:17207107
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What This Variant Does
"CLNSIG=5
Associated Conditions
Deficiency of adenosine deaminase 2
Inherited Immunodeficiency Diseases
Sneddon syndrome
Autoinflammatory syndrome
ADA2-related disorder
Deficiency of adenosine deaminase 2
Inherited Immunodeficiency Diseases
Sneddon syndrome
Autoinflammatory syndrome
ADA2-related disorder
Other Variants in ADA2
rs376785840 rs587777240 rs200930463 rs587777241 rs202134424 rs148936893 rs587777242 rs775440641 rs770689762 rs45511697
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