RS895824243 OPTN

Health Risk Chr 10:13110387
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Motor neuron disease
Amyotrophic lateral sclerosis type 12
Primary open angle glaucoma
Glaucoma 1
open angle
E
Motor neuron disease
Amyotrophic lateral sclerosis type 12
Primary open angle glaucoma
Glaucoma 1
open angle
E
Other Variants in OPTN
rs28939688 rs75654767 rs267606928 rs267606929 rs786205611 rs113811959 rs142812715 rs747481280 rs780011442 rs773095721
Ask Dr. Hemsworth about this variant