rs1555745467, CACNA1A

N. diseases: 23
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Amblyopia
CUI: C0002418
Disease: Amblyopia
0.700 GeneticVariation CLINVAR
Dehydration
CUI: C0011175
Disease: Dehydration
0.700 GeneticVariation CLINVAR
Dysarthria
CUI: C0013362
Disease: Dysarthria
0.700 GeneticVariation CLINVAR
Flatfoot
CUI: C0016202
Disease: Flatfoot
0.700 GeneticVariation CLINVAR
Tonic - clonic seizures
CUI: C0494475
Disease: Tonic - clonic seizures
0.700 GeneticVariation CLINVAR
Strabismus
CUI: C0038379
Disease: Strabismus
0.700 GeneticVariation CLINVAR
Absence Seizures
CUI: C4316903
Disease: Absence Seizures
0.700 GeneticVariation CLINVAR
Febrile Convulsions
CUI: C0009952
Disease: Febrile Convulsions
0.700 GeneticVariation CLINVAR
Poor suck
CUI: C1837142
Disease: Poor suck
0.700 GeneticVariation CLINVAR
Seizures
CUI: C0036572
Disease: Seizures
0.700 GeneticVariation CLINVAR
Sleep Apnea, Obstructive
CUI: C0520679
Disease: Sleep Apnea, Obstructive
0.700 GeneticVariation CLINVAR
Cerebellar atrophy
CUI: C0740279
Disease: Cerebellar atrophy
0.700 GeneticVariation CLINVAR
Constipation
CUI: C0009806
Disease: Constipation
0.700 GeneticVariation CLINVAR
Global developmental delay
CUI: C0557874
Disease: Global developmental delay
0.700 GeneticVariation CLINVAR
Hemiplegia/hemiparesis
CUI: C0375206
Disease: Hemiplegia/hemiparesis
0.700 GeneticVariation CLINVAR
Muscle hypotonia
CUI: C0026827
Disease: Muscle hypotonia
0.700 GeneticVariation CLINVAR
Prolonged neonatal jaundice
CUI: C1859236
Disease: Prolonged neonatal jaundice
0.700 GeneticVariation CLINVAR
Stroke-like episode
CUI: C1857287
Disease: Stroke-like episode
0.700 GeneticVariation CLINVAR
Cerebellar Ataxia
CUI: C0007758
Disease: Cerebellar Ataxia
0.700 GeneticVariation CLINVAR
Hay fever
CUI: C0018621
Disease: Hay fever
0.700 GeneticVariation CLINVAR
Hyperopia
CUI: C0020490
Disease: Hyperopia
0.700 GeneticVariation CLINVAR
Intention tremor
CUI: C4551520
Disease: Intention tremor
0.700 GeneticVariation CLINVAR
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 1
CUI: C3887485
Disease: MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 1
0.700 GeneticVariation CLINVAR