RS267606977 PRKAG2

Health Risk Chr 7:151560613
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hypertrophic cardiomyopathy 6
Lethal congenital glycogen storage disease of heart
Hypertrophic cardiomyopathy
Cardiovascular phenotype
Hypertrophic cardiomyopathy 6
Lethal congenital glycogen storage disease of heart
Hypertrophic cardiomyopathy
Cardiovascular phenotype
Other Variants in PRKAG2
rs121908987 rs121908988 rs587776643 rs28938173 rs121908989 rs121908990 rs121908991 rs267606976 rs267606978 rs193922696
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