RS786204620 ASPA

Health Risk Chr 17:3481610
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What This Variant Does
"CLNSIG=4
Associated Conditions
Spongy degeneration of central nervous system
Inborn genetic diseases
Spongy degeneration of central nervous system
Inborn genetic diseases
Other Variants in ASPA
rs28940279 rs104894548 rs28940574 rs104894549 rs12948217 rs104894550 rs2543636027 rs104894551 rs104894552 rs104894553
Ask Dr. Hemsworth about this variant