RS138958687 ATP7A
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Menkes kinky-hair syndrome
Cutis laxa
X-linked
X-linked distal spinal muscular atrophy type 3
Ehlers-Danlos syndrome
Inborn genetic diseases
ATP7A-related disorder
Menkes kinky-hair syndrome
Cutis laxa
X-linked
X-linked distal spinal muscular atrophy type 3
Ehlers-Danlos syndrome
Inborn genetic diseases
ATP7A-related disorder
Other Variants in ATP7A