RS373645939 ASNS
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
ASNS-related disorder
Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
ASNS-related disorder
Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
Other Variants in ASNS