RS769236847 ASNS
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
Neurodevelopmental delay
Pancreatic adenocarcinoma
Gastric cancer
Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
Neurodevelopmental delay
Pancreatic adenocarcinoma
Gastric cancer
Other Variants in ASNS