rs587782868, APC

N. diseases: 5
Disease: Atrial Premature Complexes ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Atrial Premature Complexes
CUI: C0033036
Disease: Atrial Premature Complexes
0.010 GeneticVariation BEFREE One homozygous MYH mutation carrier (G382D) was detected among the six patients without a family history and without a germline APC mutation who were tested. 15951963 2005