RS398122974 ASNS

Health Risk Chr 7:97852297
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=255
Associated Conditions
Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
Other Variants in ASNS
rs398122973 rs398122975 rs754043007 rs797045307 rs797045306 rs568570377 rs1057518341 rs148111963 rs773348232 rs769236847
Ask Dr. Hemsworth about this variant