RS121908990 PRKAG2

Health Risk Chr 7:151560611
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Wolff-Parkinson-White syndrome
childhood-onset
Cardiovascular phenotype
Lethal congenital glycogen storage disease of heart
Wolff-Parkinson-White syndrome
childhood-onset
Cardiovascular phenotype
Lethal congenital glycogen storage disease of heart
Other Variants in PRKAG2
rs121908987 rs121908988 rs587776643 rs28938173 rs121908989 rs121908991 rs267606976 rs267606977 rs267606978 rs193922696
Ask Dr. Hemsworth about this variant