rs1563945076, APTX

N. diseases: 4
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Torticollis
CUI: C0040485
Disease: Torticollis
0.700 CausalMutation CLINVAR
Dyskinetic syndrome
CUI: C0013384
Disease: Dyskinetic syndrome
0.700 CausalMutation CLINVAR
ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA
CUI: C1859598
Disease: ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA
0.700 CausalMutation CLINVAR
Cerebellar Ataxia
CUI: C0007758
Disease: Cerebellar Ataxia
0.700 CausalMutation CLINVAR