Gene: PRKAG2 ×
Source: UNIPROT ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121908987
rs121908987
PRKAG2
0.810 GeneticVariation UNIPROT CBS domains form energy-sensing modules whose binding of adenosine ligands is disrupted by disease mutations. 14722619

2004
dbSNP: rs121908987
rs121908987
PRKAG2
0.810 GeneticVariation UNIPROT Novel PRKAG2 mutation responsible for the genetic syndrome of ventricular preexcitation and conduction system disease with childhood onset and absence of cardiac hypertrophy. 11748095

2001
dbSNP: rs121908987
rs121908987
PRKAG2
0.810 GeneticVariation UNIPROT Identification of a gene responsible for familial Wolff-Parkinson-White syndrome. 11407343

2001
dbSNP: rs121908990
rs121908990
PRKAG2
0.700 GeneticVariation UNIPROT CBS domains form energy-sensing modules whose binding of adenosine ligands is disrupted by disease mutations. 14722619

2004
dbSNP: rs121908990
rs121908990
PRKAG2
0.700 GeneticVariation UNIPROT Identification of a gene responsible for familial Wolff-Parkinson-White syndrome. 11407343

2001
dbSNP: rs121908990
rs121908990
PRKAG2
0.700 GeneticVariation UNIPROT Novel PRKAG2 mutation responsible for the genetic syndrome of ventricular preexcitation and conduction system disease with childhood onset and absence of cardiac hypertrophy. 11748095

2001