RS104894553 ASPA

Health Risk Chr 17:3476371
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What This Variant Does
"[OMIM:?]
Associated Conditions
Mild Canavan disease
Spongy degeneration of central nervous system
Inborn genetic diseases
Canavan Disease
Familial Form
Mild Canavan disease
Spongy degeneration of central nervous system
Inborn genetic diseases
Canavan Disease
Familial Form
Other Variants in ASPA
rs28940279 rs104894548 rs28940574 rs104894549 rs12948217 rs104894550 rs2543636027 rs104894551 rs104894552 rs63751297
Ask Dr. Hemsworth about this variant