Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10428132
rs10428132
Entrez Id: 6336
Gene Symbol: SCN10A
SCN10A
CUI: C1142166
Disease:
Brugada Syndrome (disorder) 		0.830 GeneticVariation BEFREE <b>Introduction:</b> A previous genome-wide association study found three genetic loci, rs9388451, rs10428132, and rs11708996, to increase the risk of Brugada Syndrome (BrS). 30042696 2018
dbSNP: rs10428132
rs10428132
Entrez Id: 6336
Gene Symbol: SCN10A
SCN10A
CUI: C1142166
Disease:
Brugada Syndrome (disorder) 		0.830 GeneticVariation BEFREE Both rs10428132 and rs9388451 were significantly associated with BrS (P=2.7×10(-14); odds ratio, 3.0; P=9.2×10(-4); odds ratio, 1.7, respectively). 26729854 2016
dbSNP: rs10428132
rs10428132
Entrez Id: 6336
Gene Symbol: SCN10A
SCN10A
CUI: C1142166
Disease:
Brugada Syndrome (disorder) 		0.830 GeneticVariation BEFREE We investigated whether three single-nucleotide polymorphisms (SNPs) (rs11708996; G>C located intronic to SCN5A, rs10428132; T>G located in SCN10A, and rs9388451; T>C located downstream to HEY2) at loci associated with BrS in a recent genome-wide association study (GWAS) also were associated with AF. 24667784 2014
dbSNP: rs10428132
rs10428132
Entrez Id: 6336
Gene Symbol: SCN10A
SCN10A
CUI: C1142166
Disease:
Brugada Syndrome (disorder) 		T 0.830 GeneticVariation GWASDB Through a genome-wide association study of 312 individuals with Brugada syndrome and 1,115 controls, we detected 2 significant association signals at the SCN10A locus (rs10428132) and near the HEY2 gene (rs9388451). 23872634 2013
dbSNP: rs10428132
rs10428132
Entrez Id: 6336
Gene Symbol: SCN10A
SCN10A
CUI: C1142166
Disease:
Brugada Syndrome (disorder) 		T 0.830 GeneticVariation GWASCAT Through a genome-wide association study of 312 individuals with Brugada syndrome and 1,115 controls, we detected 2 significant association signals at the SCN10A locus (rs10428132) and near the HEY2 gene (rs9388451). 23872634 2013
dbSNP: rs6795970
rs6795970
Entrez Id: 6336
Gene Symbol: SCN10A
SCN10A
CUI: C0429087
Disease:
Electrocardiogram: P-R interval 		0.800 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
dbSNP: rs6798015
rs6798015
Entrez Id: 6336
Gene Symbol: SCN10A
SCN10A
CUI: C0429087
Disease:
Electrocardiogram: P-R interval 		0.800 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
dbSNP: rs6800541
rs6800541
Entrez Id: 6336
Gene Symbol: SCN10A
SCN10A
CUI: C0429087
Disease:
Electrocardiogram: P-R interval 		0.800 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
dbSNP: rs6801957
rs6801957
Entrez Id: 6336
Gene Symbol: SCN10A
SCN10A
CUI: C0429087
Disease:
Electrocardiogram: P-R interval 		C 0.800 GeneticVariation GWASCAT Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits. 30679814 2019
dbSNP: rs6801957
rs6801957
Entrez Id: 6336
Gene Symbol: SCN10A
SCN10A
CUI: C0429087
Disease:
Electrocardiogram: P-R interval 		0.800 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
dbSNP: rs7433306
rs7433306
Entrez Id: 6336
Gene Symbol: SCN10A
SCN10A
CUI: C0429087
Disease:
Electrocardiogram: P-R interval 		0.800 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
dbSNP: rs6599250
rs6599250
Entrez Id: 6336
Gene Symbol: SCN10A
SCN10A
CUI: C0429087
Disease:
Electrocardiogram: P-R interval 		T 0.800 GeneticVariation GWASCAT PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity. 30046033 2018
dbSNP: rs6801957
rs6801957
Entrez Id: 6336
Gene Symbol: SCN10A
SCN10A
CUI: C0429087
Disease:
Electrocardiogram: P-R interval 		T 0.800 GeneticVariation GWASCAT Genome-wide association study of PR interval in Hispanics/Latinos identifies novel locus at ID2. 29127183 2018
dbSNP: rs6801957
rs6801957
Entrez Id: 6336
Gene Symbol: SCN10A
SCN10A
CUI: C0429087
Disease:
Electrocardiogram: P-R interval 		T 0.800 GeneticVariation GWASCAT Genome-wide association study of electrocardiographic parameters identifies a new association for PR interval and confirms previously reported associations. 25055868 2014
dbSNP: rs7433306
rs7433306
Entrez Id: 6336
Gene Symbol: SCN10A
SCN10A
CUI: C0429087
Disease:
Electrocardiogram: P-R interval 		C 0.800 GeneticVariation GWASCAT Identification of three novel genetic variations associated with electrocardiographic traits (QRS duration and PR interval) in East Asians. 25035420 2014
dbSNP: rs138404783
rs138404783
Entrez Id: 6336
Gene Symbol: SCN10A
SCN10A
CUI: C3809893
Disease:
EPISODIC PAIN SYNDROME, FAMILIAL, 2 		0.800 GeneticVariation UNIPROT Gain-of-function Nav1.8 mutations in painful neuropathy. 23115331 2012
dbSNP: rs6801957
rs6801957
Entrez Id: 6336
Gene Symbol: SCN10A
SCN10A
CUI: C0429087
Disease:
Electrocardiogram: P-R interval 		T 0.800 GeneticVariation GWASCAT Novel loci associated with PR interval in a genome-wide association study of 10 African American cohorts. 23139255 2012
dbSNP: rs6801957
rs6801957
Entrez Id: 6336
Gene Symbol: SCN10A
SCN10A
CUI: C0429087
Disease:
Electrocardiogram: P-R interval 		T 0.800 GeneticVariation GWASDB Novel loci associated with PR interval in a genome-wide association study of 10 African American cohorts. 23139255 2012
dbSNP: rs6599250
rs6599250
Entrez Id: 6336
Gene Symbol: SCN10A
SCN10A
CUI: C0429087
Disease:
Electrocardiogram: P-R interval 		0.800 GeneticVariation GWASDB Genome-wide association studies of the PR interval in African Americans. 21347284 2011
dbSNP: rs6795970
rs6795970
Entrez Id: 6336
Gene Symbol: SCN10A
SCN10A
CUI: C0429087
Disease:
Electrocardiogram: P-R interval 		0.800 GeneticVariation GWASDB Genome-wide association studies of the PR interval in African Americans. 21347284 2011
dbSNP: rs6798015
rs6798015
Entrez Id: 6336
Gene Symbol: SCN10A
SCN10A
CUI: C0429087
Disease:
Electrocardiogram: P-R interval 		C 0.800 GeneticVariation GWASCAT Genome-wide association studies of the PR interval in African Americans. 21347284 2011
dbSNP: rs6798015
rs6798015
Entrez Id: 6336
Gene Symbol: SCN10A
SCN10A
CUI: C0429087
Disease:
Electrocardiogram: P-R interval 		0.800 GeneticVariation GWASDB Genome-wide association studies of the PR interval in African Americans. 21347284 2011
dbSNP: rs6800541
rs6800541
Entrez Id: 6336
Gene Symbol: SCN10A
SCN10A
CUI: C0429087
Disease:
Electrocardiogram: P-R interval 		0.800 GeneticVariation GWASDB Genome-wide association studies of the PR interval in African Americans. 21347284 2011
dbSNP: rs6801957
rs6801957
Entrez Id: 6336
Gene Symbol: SCN10A
SCN10A
CUI: C0429087
Disease:
Electrocardiogram: P-R interval 		0.800 GeneticVariation GWASDB Genome-wide association studies of the PR interval in African Americans. 21347284 2011
dbSNP: rs7433306
rs7433306
Entrez Id: 6336
Gene Symbol: SCN10A
SCN10A
CUI: C0429087
Disease:
Electrocardiogram: P-R interval 		0.800 GeneticVariation GWASDB Genome-wide association studies of the PR interval in African Americans. 21347284 2011