RS886043860 SGCG

Health Risk Chr 13:23320657
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive limb-girdle muscular dystrophy type 2C
Autosomal recessive limb-girdle muscular dystrophy type 2C
Other Variants in SGCG
rs2137534216 rs104894422 rs762777463 rs104894423 rs786204786 rs763248287 rs144497243 rs797044783 rs797045106 rs875989949
Ask Dr. Hemsworth about this variant