Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137854600
rs137854600
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C1859062
Disease:
LONG QT SYNDROME 3
T 0.840 CausalMutation CLINVAR
dbSNP: rs137854601
rs137854601
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C1859062
Disease:
LONG QT SYNDROME 3
T 0.820 GeneticVariation CLINVAR
dbSNP: rs137854614
rs137854614
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C1859062
Disease:
LONG QT SYNDROME 3
C 0.810 CausalMutation CLINVAR
dbSNP: rs199473283
rs199473283
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C1859062
Disease:
LONG QT SYNDROME 3
T 0.810 GeneticVariation CLINVAR
dbSNP: rs199473311
rs199473311
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C1859062
Disease:
LONG QT SYNDROME 3
C 0.810 CausalMutation CLINVAR
dbSNP: rs199473603
rs199473603
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C1859062
Disease:
LONG QT SYNDROME 3
A 0.810 GeneticVariation CLINVAR
dbSNP: rs137854601
rs137854601
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C4551804
Disease:
Brugada Syndrome 1
T 0.800 CausalMutation CLINVAR
dbSNP: rs137854602
rs137854602
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C4551804
Disease:
Brugada Syndrome 1
A 0.800 GeneticVariation CLINVAR
dbSNP: rs137854602
rs137854602
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C4551804
Disease:
Brugada Syndrome 1
A 0.800 CausalMutation CLINVAR
dbSNP: rs137854603
rs137854603
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C4551804
Disease:
Brugada Syndrome 1
T 0.800 CausalMutation CLINVAR
dbSNP: rs137854605
rs137854605
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C1859062
Disease:
LONG QT SYNDROME 3
TT 0.800 CausalMutation CLINVAR
dbSNP: rs137854607
rs137854607
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C1879286
Disease:
Hereditary bundle branch system defect
T 0.800 CausalMutation CLINVAR
dbSNP: rs137854609
rs137854609
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C1859062
Disease:
LONG QT SYNDROME 3
A 0.800 CausalMutation CLINVAR
dbSNP: rs137854611
rs137854611
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C4551804
Disease:
Brugada Syndrome 1
A 0.800 CausalMutation CLINVAR
dbSNP: rs137854612
rs137854612
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C4551804
Disease:
Brugada Syndrome 1
T 0.800 CausalMutation CLINVAR
dbSNP: rs137854612
rs137854612
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C1837845
Disease:
SICK SINUS SYNDROME 1, AUTOSOMAL RECESSIVE
T 0.800 CausalMutation CLINVAR
dbSNP: rs137854615
rs137854615
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C4551804
Disease:
Brugada Syndrome 1
G 0.800 CausalMutation CLINVAR
dbSNP: rs137854617
rs137854617
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C4551804
Disease:
Brugada Syndrome 1
T 0.800 CausalMutation CLINVAR
dbSNP: rs137854617
rs137854617
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C1859062
Disease:
LONG QT SYNDROME 3
T 0.800 GeneticVariation CLINVAR
dbSNP: rs137854617
rs137854617
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C3151464
Disease:
ATRIAL FIBRILLATION, FAMILIAL, 10
T 0.800 CausalMutation CLINVAR
dbSNP: rs137854618
rs137854618
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C1832680
Disease:
CARDIOMYOPATHY, DILATED, 1E
T 0.800 CausalMutation CLINVAR
dbSNP: rs199473072
rs199473072
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C1859062
Disease:
LONG QT SYNDROME 3
A 0.800 CausalMutation CLINVAR
dbSNP: rs199473083
rs199473083
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C4551804
Disease:
Brugada Syndrome 1
T 0.800 CausalMutation CLINVAR
dbSNP: rs199473097
rs199473097
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C1859062
Disease:
LONG QT SYNDROME 3
A 0.800 CausalMutation CLINVAR
dbSNP: rs199473097
rs199473097
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C4551804
Disease:
Brugada Syndrome 1
A 0.800 CausalMutation CLINVAR