RS757681143 PYGM

Health Risk Chr 11:64753971
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Glycogen storage disease
type V
PYGM-related disorder
Glycogen storage disease
type V
PYGM-related disorder
Other Variants in PYGM
rs116987552 rs119103251 rs119103252 rs119103253 rs119103256 rs119103254 rs144081869 rs119103255 rs786200874 rs267606993
Ask Dr. Hemsworth about this variant