RS376712636 SEPTIN9

Health Risk Chr 17:77492700
Upload your DNA to see your genotype for this variant.
Associated Conditions
Charcot-Marie-Tooth disease
type I
Amyotrophic neuralgia
Charcot-Marie-Tooth disease
type I
Amyotrophic neuralgia
Other Variants in SEPTIN9
rs80338761 rs80338762 rs80338760 rs769442066 rs199861986 rs201560726 rs544797046 rs200031107 rs886053495 rs539303139
Ask Dr. Hemsworth about this variant