RS104894635 SGSH

Health Risk Chr 17:80213815
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What This Variant Does
"rs104894635, also known as c.734G&gt
Associated Conditions
Mucopolysaccharidosis
MPS-III-A
Sanfilippo syndrome
Inborn genetic diseases
Neurodegeneration
SGSH-related disorder
Mucopolysaccharidosis
MPS-III-A
Mucopolysaccharidosis
MPS-III-A
Sanfilippo syndrome
Inborn genetic diseases
Neurodegeneration
SGSH-related disorder
Mucopolysaccharidosis
Other Variants in SGSH
rs104894636 rs104894641 rs104894642 rs104894637 rs104894638 rs104894639 rs104894640 rs104894643 rs138504221 rs398123244
Ask Dr. Hemsworth about this variant