RS786204786 SGCG

Health Risk Chr 13:23295430
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
SGCG-related congenital myopathy
Autosomal recessive limb-girdle muscular dystrophy
Autosomal recessive limb-girdle muscular dystrophy type 2C
SGCG-related congenital myopathy
Autosomal recessive limb-girdle muscular dystrophy
Other Variants in SGCG
rs2137534216 rs104894422 rs762777463 rs104894423 rs763248287 rs144497243 rs797044783 rs797045106 rs875989949 rs140810408
Ask Dr. Hemsworth about this variant