RS771427957 PYGM

Health Risk Chr 11:64751923
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Glycogen storage disease
type V
Inborn genetic diseases
Glycogen storage disease
type V
Other Variants in PYGM
rs116987552 rs119103251 rs119103252 rs119103253 rs119103256 rs119103254 rs144081869 rs119103255 rs786200874 rs267606993
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