RS202079794 SEPTIN9

Health Risk Chr 17:77402208
Upload your DNA to see your genotype for this variant.
Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in SEPTIN9
rs80338761 rs80338762 rs80338760 rs769442066 rs199861986 rs201560726 rs544797046 rs200031107 rs886053495 rs539303139
Ask Dr. Hemsworth about this variant