Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs199472936
rs199472936
KCNH2
0.010 GeneticVariation BEFREE We recently reported a novel missense mutation of HERG (G601S) in an LQTS family that we have characterized in the present work. 10226095

1999