RS104894641 SGSH

Health Risk Chr 17:80210663
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What This Variant Does
"[OMIM:?]
Associated Conditions
Mucopolysaccharidosis
MPS-III-A
Inborn genetic diseases
Mucopolysaccharidosis
MPS-III-A
Inborn genetic diseases
Other Variants in SGSH
rs104894635 rs104894636 rs104894642 rs104894637 rs104894638 rs104894639 rs104894640 rs104894643 rs138504221 rs398123244
Ask Dr. Hemsworth about this variant