RS398122973 ASNS

Health Risk Chr 7:97855406
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What This Variant Does
"CLNSIG=5
Associated Conditions
Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
Other Variants in ASNS
rs398122974 rs398122975 rs754043007 rs797045307 rs797045306 rs568570377 rs1057518341 rs148111963 rs773348232 rs769236847
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