Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs199473115
rs199473115
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C3151464
Disease:
ATRIAL FIBRILLATION, FAMILIAL, 10
C 0.800 CausalMutation CLINVAR
dbSNP: rs199473121
rs199473121
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C1859062
Disease:
LONG QT SYNDROME 3
T 0.800 CausalMutation CLINVAR
dbSNP: rs199473171
rs199473171
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C4551804
Disease:
Brugada Syndrome 1
A 0.800 GeneticVariation CLINVAR
dbSNP: rs199473266
rs199473266
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C1859062
Disease:
LONG QT SYNDROME 3
C 0.800 GeneticVariation CLINVAR
dbSNP: rs199473282
rs199473282
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C4551804
Disease:
Brugada Syndrome 1
A 0.800 CausalMutation CLINVAR
dbSNP: rs199473310
rs199473310
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C1859062
Disease:
LONG QT SYNDROME 3
A 0.800 CausalMutation CLINVAR
dbSNP: rs199473556
rs199473556
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C4551804
Disease:
Brugada Syndrome 1
A 0.800 CausalMutation CLINVAR
dbSNP: rs199473565
rs199473565
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C4551804
Disease:
Brugada Syndrome 1
T 0.800 CausalMutation CLINVAR
dbSNP: rs199473579
rs199473579
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C3151464
Disease:
ATRIAL FIBRILLATION, FAMILIAL, 10
T 0.800 CausalMutation CLINVAR
dbSNP: rs199473620
rs199473620
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C4551804
Disease:
Brugada Syndrome 1
A 0.800 CausalMutation CLINVAR
dbSNP: rs28937317
rs28937317
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C1859062
Disease:
LONG QT SYNDROME 3
C 0.800 CausalMutation CLINVAR
dbSNP: rs28937318
rs28937318
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C4551804
Disease:
Brugada Syndrome 1
T 0.800 CausalMutation CLINVAR
dbSNP: rs28937319
rs28937319
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C1837845
Disease:
SICK SINUS SYNDROME 1, AUTOSOMAL RECESSIVE
A 0.800 CausalMutation CLINVAR
dbSNP: rs45546039
rs45546039
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C4551804
Disease:
Brugada Syndrome 1
T 0.800 CausalMutation CLINVAR
dbSNP: rs45546039
rs45546039
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C1859062
Disease:
LONG QT SYNDROME 3
T 0.800 CausalMutation CLINVAR
dbSNP: rs45620037
rs45620037
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C1837845
Disease:
SICK SINUS SYNDROME 1, AUTOSOMAL RECESSIVE
A 0.800 CausalMutation CLINVAR
dbSNP: rs45620037
rs45620037
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C1837845
Disease:
SICK SINUS SYNDROME 1, AUTOSOMAL RECESSIVE
0.800 GeneticVariation UNIPROT
dbSNP: rs7626962
rs7626962
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C0038644
Disease:
Sudden infant death syndrome
T 0.750 CausalMutation CLINVAR
dbSNP: rs137854611
rs137854611
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C1142166
Disease:
Brugada Syndrome (disorder)
A 0.710 GeneticVariation CLINVAR
dbSNP: rs199473062
rs199473062
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C1142166
Disease:
Brugada Syndrome (disorder)
T 0.710 CausalMutation CLINVAR
dbSNP: rs199473603
rs199473603
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C0023976
Disease:
Long QT Syndrome
A 0.710 GeneticVariation CLINVAR
dbSNP: rs759924541
rs759924541
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C1142166
Disease:
Brugada Syndrome (disorder)
T 0.710 CausalMutation CLINVAR
dbSNP: rs1057518916
rs1057518916
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C0039070
Disease:
Syncope
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1060501114
rs1060501114
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C1142166
Disease:
Brugada Syndrome (disorder)
T 0.700 CausalMutation CLINVAR
dbSNP: rs1060501127
rs1060501127
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C1142166
Disease:
Brugada Syndrome (disorder)
C 0.700 GeneticVariation CLINVAR