RS387906709 UBQLN2
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What This Variant Does
"Two causative, dominantly inherited mutations have been mapped to this location on the X chromosome:...
Associated Conditions
Amyotrophic lateral sclerosis type 15
Amyotrophic lateral sclerosis type 15
Amyotrophic lateral sclerosis type 15
Amyotrophic lateral sclerosis type 15
Other Variants in UBQLN2