RS369947678 UBQLN2

Health Risk Chr X:56565446
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Amyotrophic lateral sclerosis type 15
Amyotrophic lateral sclerosis
UBQLN2-related disorder
Amyotrophic lateral sclerosis type 15
Amyotrophic lateral sclerosis
UBQLN2-related disorder
Other Variants in UBQLN2
rs1360902821 rs143098023 rs763761196 rs1164344738 rs2519963370 rs1470922571 rs143736302 rs746075271 rs201549050 rs387906709
Ask Dr. Hemsworth about this variant