RS104894176 PRF1

Health Risk Chr 10:70598599
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Familial hemophagocytic lymphohistiocytosis 2
Autoinflammatory syndrome
Inborn genetic diseases
Aplastic anemia
Lymphoma
non-Hodgkin
familial
Familial hemophagocytic lymphohistiocytosis 2
Autoinflammatory syndrome
Inborn genetic diseases
Aplastic anemia
Lymphoma
non-Hodgkin
familial
Other Variants in PRF1
rs104894180 rs28933973 rs104894182 rs104894183 rs28933376 rs35947132 rs771552960 rs786205093 rs193302876 rs751161742
Ask Dr. Hemsworth about this variant