RS116180923 PYGM

Health Risk Chr 11:64751369 snv missense variant
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Associated Conditions
Glycogen storage disease
type V
Inborn genetic diseases
Glycogen storage disease
type V
Inborn genetic diseases
Population Frequencies
gnomAD ALL
0%
1kG AFR
99.7%
1kG ALL
99.9%
1kG AMR
0.1%
1kG EAS
100%
1kG EUR
100%
1kG SAS
100%
Other Variants in PYGM
rs116987552 rs119103251 rs119103252 rs119103253 rs119103256 rs119103254 rs144081869 rs119103255 rs786200874 rs267606993
Ask Dr. Hemsworth about this variant