Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1553700699
rs1553700699
SCN5A
T 0.700 CausalMutation CLINVAR Heterozygous nonsense SCN5A mutation W822X explains a simultaneous sudden infant death syndrome. 18551308

2008
dbSNP: rs1553700699
rs1553700699
SCN5A
T 0.700 CausalMutation CLINVAR A novel nonsense mutation in the SCN5A gene leads to Brugada syndrome and a silent gene mutation carrier state. 16239976

2005