Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs114925667
rs114925667
Entrez Id: 79876;100532724
Gene Symbol: UBA5;NPHP3-ACAD11
UBA5;NPHP3-ACAD11
CUI: C0271385
Disease:
Horizontal Nystagmus
A 0.700 CausalMutation CLINVAR
dbSNP: rs1553770577
rs1553770577
Entrez Id: 79876;100532724
Gene Symbol: UBA5;NPHP3-ACAD11
UBA5;NPHP3-ACAD11
CUI: C0271385
Disease:
Horizontal Nystagmus
C 0.700 GeneticVariation CLINVAR