RS12948217 ASPA

Health Risk Chr 17:3494408
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What This Variant Does
"rs12948217, also known as c.693C&gt
Associated Conditions
Spongy degeneration of central nervous system
Canavan Disease
Familial Form
Inborn genetic diseases
ASPA-related disorder
Spongy degeneration of central nervous system
Canavan Disease
Familial Form
Inborn genetic diseases
ASPA-related disorder
Other Variants in ASPA
rs28940279 rs104894548 rs28940574 rs104894549 rs104894550 rs2543636027 rs104894551 rs104894552 rs104894553 rs63751297
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