RS746332433 AMPD2

Health Risk Chr 1:109627794
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Pontocerebellar hypoplasia type 9
Hereditary spastic paraplegia 63
Inborn genetic diseases
Inborn genetic diseases
Pontocerebellar hypoplasia type 9
Hereditary spastic paraplegia 63
Inborn genetic diseases
Other Variants in AMPD2
rs587777769 rs587777391 rs587777392 rs587777393 rs587777394 rs587777395 rs192669225 rs114727970 rs869312928 rs875989844
Ask Dr. Hemsworth about this variant