Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs751751942
rs751751942
Entrez Id: 29098;399512
Gene Symbol: RANGRF;SLC25A35
RANGRF;SLC25A35
CUI: C1142166
Disease:
Brugada Syndrome (disorder) 		0.020 GeneticVariation BEFREE In conclusion, our findings identify the structural elements in MOG1 that are crucial for its interaction with Na<sub>v</sub>1.5 and improve our understanding of how the E83D substitution causes BrS. 30282806 2018
dbSNP: rs751751942
rs751751942
Entrez Id: 29098;399512
Gene Symbol: RANGRF;SLC25A35
RANGRF;SLC25A35
CUI: C1142166
Disease:
Brugada Syndrome (disorder) 		0.020 GeneticVariation BEFREE A missense mutation p.Glu83Asp (E83D) was detected in a symptomatic female patient with a type-1 BrS ECG but not in 281 controls. 21447824 2011
dbSNP: rs140704891
rs140704891
Entrez Id: 29098;399512
Gene Symbol: RANGRF;SLC25A35
RANGRF;SLC25A35
CUI: C1142166
Disease:
Brugada Syndrome (disorder) 		0.010 GeneticVariation BEFREE We suggest that p.E61X_RANGRF is a rare genetic variation with an uncertain role in Br</span>ugada Syndrome</span>. 24142675 2014
dbSNP: rs370613922
rs370613922
Entrez Id: 29098;399512
Gene Symbol: RANGRF;SLC25A35
RANGRF;SLC25A35
CUI: C1142166
Disease:
Brugada Syndrome (disorder) 		0.010 GeneticVariation BEFREE Three SCN5A mutations (V95I, R121Q, and R367H) have been previously implicated in BrS. 24529773 2014