Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs767910122
rs767910122
KCNH2
CUI: C0023976
Disease: Long QT Syndrome
Long QT Syndrome 		0.020 GeneticVariation BEFREE Our data suggest that a common polymorphism (K897T) can markedly accentuate the loss of function of mildly defective HERG channels, leading to long-QT syndrome-mediated arrhythmias and sudden infant death. 20181576

2010
dbSNP: rs767910122
rs767910122
KCNH2
CUI: C0023976
Disease: Long QT Syndrome
Long QT Syndrome 		0.020 GeneticVariation BEFREE Our family-based approach provides support that KCNH2 SNP K897T confers a protective effect on LQTS patients. 18808722

2008