Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12720459
rs12720459
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C4551647
Disease:
Long QT Syndrome 1
A 0.850 CausalMutation CLINVAR
dbSNP: rs12720459
rs12720459
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C4551647
Disease:
Long QT Syndrome 1
T 0.850 CausalMutation CLINVAR
dbSNP: rs120074178
rs120074178
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C4551647
Disease:
Long QT Syndrome 1
A 0.810 CausalMutation CLINVAR
dbSNP: rs120074178
rs120074178
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C4551647
Disease:
Long QT Syndrome 1
T 0.810 CausalMutation CLINVAR
dbSNP: rs120074191
rs120074191
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C4551647
Disease:
Long QT Syndrome 1
T 0.810 CausalMutation CLINVAR
dbSNP: rs120074193
rs120074193
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C4551647
Disease:
Long QT Syndrome 1
A 0.810 CausalMutation CLINVAR
dbSNP: rs199472755
rs199472755
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C4551647
Disease:
Long QT Syndrome 1
A 0.810 GeneticVariation CLINVAR
dbSNP: rs199473457
rs199473457
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C4551647
Disease:
Long QT Syndrome 1
T 0.810 CausalMutation CLINVAR
dbSNP: rs104894252
rs104894252
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C4551647
Disease:
Long QT Syndrome 1
A 0.800 CausalMutation CLINVAR
dbSNP: rs120074177
rs120074177
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C4551647
Disease:
Long QT Syndrome 1
C 0.800 CausalMutation CLINVAR
dbSNP: rs120074179
rs120074179
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C4551647
Disease:
Long QT Syndrome 1
A 0.800 CausalMutation CLINVAR
dbSNP: rs120074180
rs120074180
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C4551647
Disease:
Long QT Syndrome 1
T 0.800 CausalMutation CLINVAR
dbSNP: rs120074181
rs120074181
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C4551647
Disease:
Long QT Syndrome 1
A 0.800 CausalMutation CLINVAR
dbSNP: rs120074182
rs120074182
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C4551647
Disease:
Long QT Syndrome 1
T 0.800 CausalMutation CLINVAR
dbSNP: rs120074183
rs120074183
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C4551647
Disease:
Long QT Syndrome 1
A 0.800 CausalMutation CLINVAR
dbSNP: rs120074184
rs120074184
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C4551647
Disease:
Long QT Syndrome 1
A 0.800 CausalMutation CLINVAR
dbSNP: rs120074185
rs120074185
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C4551647
Disease:
Long QT Syndrome 1
T 0.800 CausalMutation CLINVAR
dbSNP: rs120074186
rs120074186
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C4551509
Disease:
Jervell And Lange-Nielsen Syndrome 1
C 0.800 CausalMutation CLINVAR
dbSNP: rs120074187
rs120074187
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C4551647
Disease:
Long QT Syndrome 1
A 0.800 GeneticVariation CLINVAR
dbSNP: rs120074187
rs120074187
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C4551647
Disease:
Long QT Syndrome 1
A 0.800 CausalMutation CLINVAR
dbSNP: rs120074190
rs120074190
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C4551509
Disease:
Jervell And Lange-Nielsen Syndrome 1
A 0.800 CausalMutation CLINVAR
dbSNP: rs120074190
rs120074190
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C4551647
Disease:
Long QT Syndrome 1
A 0.800 CausalMutation CLINVAR
dbSNP: rs120074192
rs120074192
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C1837014
Disease:
Atrial Fibrillation, Familial, 3
G 0.800 CausalMutation CLINVAR
dbSNP: rs120074194
rs120074194
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C4551647
Disease:
Long QT Syndrome 1
A 0.800 CausalMutation CLINVAR
dbSNP: rs120074195
rs120074195
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C1865019
Disease:
SHORT QT SYNDROME 2 (disorder)
C 0.800 CausalMutation CLINVAR