RS144982168 AARS1

Health Risk Chr 16:70262353
Upload your DNA to see your genotype for this variant.
Associated Conditions
Charcot-Marie-Tooth disease type 2
Inborn genetic diseases
Trichothiodystrophy 8
nonphotosensitive
Developmental and epileptic encephalopathy
29
Charcot-Marie-Tooth disease type 2
Inborn genetic diseases
Trichothiodystrophy 8
nonphotosensitive
Developmental and epileptic encephalopathy
29
Other Variants in AARS1
rs267606621 rs387906792 rs138081804 rs786205157 rs143370729 rs200586605 rs150080663 rs137894161 rs757295540 rs369774476
Ask Dr. Hemsworth about this variant