RS770947426 SGSH

Health Risk Chr 17:80210881
Upload your DNA to see your genotype for this variant.
What This Variant Does
"rs770947426, also known as c.1080delC, represents a rare mutation in the SGSH gene on chromosome 17...."
Associated Conditions
Mucopolysaccharidosis
MPS-III-A
Mucopolysaccharidosis
MPS-III-A
Other Variants in SGSH
rs104894635 rs104894636 rs104894641 rs104894642 rs104894637 rs104894638 rs104894639 rs104894640 rs104894643 rs138504221
Ask Dr. Hemsworth about this variant