RS192669225 AMPD2

Health Risk Chr 1:109628692
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What This Variant Does
"CLNSIG=4
Associated Conditions
Global developmental delay
Brain malformation
Seizure
Hereditary spastic paraplegia 63
Pontocerebellar hypoplasia type 9
Global developmental delay
Brain malformation
Seizure
Hereditary spastic paraplegia 63
Pontocerebellar hypoplasia type 9
Other Variants in AMPD2
rs587777769 rs587777391 rs587777392 rs587777393 rs587777394 rs587777395 rs114727970 rs746332433 rs869312928 rs875989844
Ask Dr. Hemsworth about this variant