RS587777395 AMPD2

Health Risk Chr 1:109629487
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What This Variant Does
"CLNSIG=5
Associated Conditions
Pontocerebellar hypoplasia type 9
Hereditary spastic paraplegia 63
Pontoneocerebellar hypoplasia
Pontocerebellar hypoplasia type 9
Pontocerebellar hypoplasia type 9
Hereditary spastic paraplegia 63
Pontoneocerebellar hypoplasia
Pontocerebellar hypoplasia type 9
Other Variants in AMPD2
rs587777769 rs587777391 rs587777392 rs587777393 rs587777394 rs192669225 rs114727970 rs746332433 rs869312928 rs875989844
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