RS121908991 PRKAG2

Health Risk Chr 7:151560610
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What This Variant Does
"The rare minor allele of this variant is reported to be pathogenic/likely pathogenic for familial hy...
Associated Conditions
Lethal congenital glycogen storage disease of heart
Hypertrophic cardiomyopathy
Gastric cancer
Hypertrophic cardiomyopathy
Lethal congenital glycogen storage disease of heart
Cardiomyopathy
Lethal congenital glycogen storage disease of heart
Hypertrophic cardiomyopathy
Gastric cancer
Hypertrophic cardiomyopathy
Lethal congenital glycogen storage disease of heart
Cardiomyopathy
Other Variants in PRKAG2
rs121908987 rs121908988 rs587776643 rs28938173 rs121908989 rs121908990 rs267606976 rs267606977 rs267606978 rs193922696
Ask Dr. Hemsworth about this variant