RS200287925 NBN
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary cancer-predisposing syndrome
Microcephaly
normal intelligence and immunodeficiency
Gastric cancer
Aplastic anemia
Acute lymphoid leukemia
Hereditary cancer-predisposing syndrome
Microcephaly
normal intelligence and immunodeficiency
Gastric cancer
Aplastic anemia
Acute lymphoid leukemia
Other Variants in NBN