Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1345176461
rs1345176461
Entrez Id: 64207;107984638
Gene Symbol: IRF2BPL;LOC107984638
IRF2BPL;LOC107984638
CUI: C0028738
Disease:
Nystagmus
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1555377415
rs1555377415
Entrez Id: 64207;107984638
Gene Symbol: IRF2BPL;LOC107984638
IRF2BPL;LOC107984638
CUI: C0028738
Disease:
Nystagmus
C 0.700 GeneticVariation CLINVAR