Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1009298200
rs1009298200
Entrez Id: 56052
Gene Symbol: ALG1
ALG1
CUI: C0494475
Disease:
Tonic - clonic seizures
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1555452127
rs1555452127
Entrez Id: 56052
Gene Symbol: ALG1
ALG1
CUI: C0494475
Disease:
Tonic - clonic seizures
C 0.700 GeneticVariation CLINVAR
dbSNP: rs369160589
rs369160589
Entrez Id: 56052
Gene Symbol: ALG1
ALG1
CUI: C0494475
Disease:
Tonic - clonic seizures
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1009298200
rs1009298200
Entrez Id: 56052
Gene Symbol: ALG1
ALG1
CUI: C1820737
Disease:
Temperature instability
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1555452127
rs1555452127
Entrez Id: 56052
Gene Symbol: ALG1
ALG1
CUI: C1820737
Disease:
Temperature instability
C 0.700 GeneticVariation CLINVAR
dbSNP: rs369160589
rs369160589
Entrez Id: 56052
Gene Symbol: ALG1
ALG1
CUI: C1820737
Disease:
Temperature instability
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1009298200
rs1009298200
Entrez Id: 56052
Gene Symbol: ALG1
ALG1
CUI: C0426886
Disease:
Tapering fingers (finding)
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1555452127
rs1555452127
Entrez Id: 56052
Gene Symbol: ALG1
ALG1
CUI: C0426886
Disease:
Tapering fingers (finding)
C 0.700 GeneticVariation CLINVAR
dbSNP: rs369160589
rs369160589
Entrez Id: 56052
Gene Symbol: ALG1
ALG1
CUI: C0426886
Disease:
Tapering fingers (finding)
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1009298200
rs1009298200
Entrez Id: 56052
Gene Symbol: ALG1
ALG1
CUI: C0039231
Disease:
Tachycardia
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1555452127
rs1555452127
Entrez Id: 56052
Gene Symbol: ALG1
ALG1
CUI: C0039231
Disease:
Tachycardia
C 0.700 GeneticVariation CLINVAR
dbSNP: rs369160589
rs369160589
Entrez Id: 56052
Gene Symbol: ALG1
ALG1
CUI: C0039231
Disease:
Tachycardia
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1009298200
rs1009298200
Entrez Id: 56052
Gene Symbol: ALG1
ALG1
CUI: C0235991
Disease:
Small for gestational age (disorder)
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1555452127
rs1555452127
Entrez Id: 56052
Gene Symbol: ALG1
ALG1
CUI: C0235991
Disease:
Small for gestational age (disorder)
C 0.700 GeneticVariation CLINVAR
dbSNP: rs369160589
rs369160589
Entrez Id: 56052
Gene Symbol: ALG1
ALG1
CUI: C0235991
Disease:
Small for gestational age (disorder)
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1009298200
rs1009298200
Entrez Id: 56052
Gene Symbol: ALG1
ALG1
CUI: C1837397
Disease:
Severe global developmental delay
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1555452127
rs1555452127
Entrez Id: 56052
Gene Symbol: ALG1
ALG1
CUI: C1837397
Disease:
Severe global developmental delay
C 0.700 GeneticVariation CLINVAR
dbSNP: rs369160589
rs369160589
Entrez Id: 56052
Gene Symbol: ALG1
ALG1
CUI: C1837397
Disease:
Severe global developmental delay
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1009298200
rs1009298200
Entrez Id: 56052
Gene Symbol: ALG1
ALG1
CUI: C0751495
Disease:
Seizures, Focal
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1555452127
rs1555452127
Entrez Id: 56052
Gene Symbol: ALG1
ALG1
CUI: C0751495
Disease:
Seizures, Focal
C 0.700 GeneticVariation CLINVAR
dbSNP: rs369160589
rs369160589
Entrez Id: 56052
Gene Symbol: ALG1
ALG1
CUI: C0751495
Disease:
Seizures, Focal
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1009298200
rs1009298200
Entrez Id: 56052
Gene Symbol: ALG1
ALG1
CUI: C0036572
Disease:
Seizures
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1555452127
rs1555452127
Entrez Id: 56052
Gene Symbol: ALG1
ALG1
CUI: C0036572
Disease:
Seizures
C 0.700 GeneticVariation CLINVAR
dbSNP: rs369160589
rs369160589
Entrez Id: 56052
Gene Symbol: ALG1
ALG1
CUI: C0036572
Disease:
Seizures
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1009298200
rs1009298200
Entrez Id: 56052
Gene Symbol: ALG1
ALG1
CUI: C0036439
Disease:
Scoliosis, unspecified
G 0.700 GeneticVariation CLINVAR