Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs758361736
rs758361736
CUI: C0028738
Disease: Nystagmus
Nystagmus
G 0.700 CausalMutation CLINVAR

dbSNP: rs758361736
rs758361736
CUI: C0028738
Disease: Nystagmus
Nystagmus
G 0.700 GeneticVariation CLINVAR