Variant Gene Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs773724817
rs773724817
0.710 CausalMutation CLINVAR Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria. 28492532

2017

dbSNP: rs773724817
rs773724817
0.710 GeneticVariation BEFREE Clinical and electrophysiological characterization of a novel mutation R863X in HERG C-terminus associated with long QT syndrome. 14714110

2004