RS139488862 AGL

Health Risk Chr 1:99880654 snv missense variant
Upload your DNA to see your genotype for this variant.
Associated Conditions
Glycogen storage disease type III
Inborn genetic diseases
Glycogen storage disease type III
Inborn genetic diseases
Population Frequencies
gnomAD ALL
99.9%
1kG AFR
100%
1kG ALL
0%
1kG AMR
100%
1kG EAS
100%
1kG EUR
0.2%
1kG SAS
100%
Other Variants in AGL
rs387906244 rs113994126 rs113994129 rs113994134 rs369973784 rs199922945 rs118203964 rs113994132 rs387906246 rs780504025
Ask Dr. Hemsworth about this variant