RS104894450 PNP

Health Risk Chr 14:20474870
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Purine-nucleoside phosphorylase deficiency
Severe combined immunodeficiency disease
Purine-nucleoside phosphorylase deficiency
Severe combined immunodeficiency disease
Other Variants in PNP
rs104894453 rs104894454 rs104894451 rs104894452 rs2501836909 rs104894455 rs104894460 rs1566525400 rs563086985 rs367991537
Ask Dr. Hemsworth about this variant