RS730882249 AP4M1

Health Risk Chr 7:100105981
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What This Variant Does
"CLNSIG=5
Associated Conditions
CNS hypomyelination
Brain atrophy
Microcephaly
Hypoplasia of the corpus callosum
Global developmental delay
Hereditary spastic paraplegia 50
Spastic paraplegia
AP4M1-related disorder
CNS hypomyelination
Brain atrophy
Microcephaly
Hypoplasia of the corpus callosum
Global developmental delay
Hereditary spastic paraplegia 50
Spastic paraplegia
Other Variants in AP4M1
rs387906838 rs146262009 rs797045249 rs367614875 rs138437966 rs754498075 rs372787797 rs147738731 rs141754568 rs752598529
Ask Dr. Hemsworth about this variant