RS61754966 NBN
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Aplastic anemia
Leukemia
acute lymphoblastic
susceptibility to
Hereditary cancer-predisposing syndrome
Microcephaly
normal intelligence and immunodeficiency
Acute lymphoid leukemia
Hereditary breast ovarian cancer syndrome
Carcinoma of colon
Breast carcinoma
Hereditary cancer
NBN-related disorder
Diffuse midline glioma
H3 K27-altered
Other Variants in NBN