RS587777394 AMPD2

Health Risk Chr 1:109630740
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Pontocerebellar hypoplasia type 9
Pontocerebellar hypoplasia type 9
Other Variants in AMPD2
rs587777769 rs587777391 rs587777392 rs587777393 rs587777395 rs192669225 rs114727970 rs746332433 rs869312928 rs875989844
Ask Dr. Hemsworth about this variant