Disease: Acquired long QT syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs199472918
rs199472918
Entrez Id: 3757
Gene Symbol: KCNH2
KCNH2
CUI: C2732979
Disease:
Acquired long QT syndrome 		0.010 GeneticVariation BEFREE DNA samples were screened for the four common Finnish founder mutations (KCNQ1 G589D and IVS7-2A-->G, HERG L552S, and R176W), which are known to account for the majority of inherited LQTS in Finland. 17467628 2007