rs1805124, SCN5A

N. diseases: 16
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Andersen Syndrome
CUI: C1563715
Disease: Andersen Syndrome
0.010 GeneticVariation BEFREE Symptoms presented by the member with only the ATS mutation and by member with ATS mutation and H558R polymorphism were not as severe. 26109178 2016