RS138504221 SGSH

Health Risk Chr 17:80212128
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What This Variant Does
"CLNSIG=5
Associated Conditions
Mucopolysaccharidosis
MPS-III-A
Sanfilippo syndrome
7 conditions
Neurodegeneration
Cone-rod dystrophy
Inborn genetic diseases
Mucopolysaccharidosis
MPS-III-A
Sanfilippo syndrome
7 conditions
Neurodegeneration
Cone-rod dystrophy
Inborn genetic diseases
Other Variants in SGSH
rs104894635 rs104894636 rs104894641 rs104894642 rs104894637 rs104894638 rs104894639 rs104894640 rs104894643 rs398123244
Ask Dr. Hemsworth about this variant