Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121912512
rs121912512
KCNH2
CUI: C0023976
Disease: Long QT Syndrome
Long QT Syndrome 		0.710 GeneticVariation BEFREE Direct bidirectional sequencing of long QT syndrome genes identified a previously unreported HERG missense mutation (R752Q). 12621127

2003