FIGNL1, fidgetin like 1, 63979

N. diseases: 23; N. variants: 60
Disease: Paroxysmal involuntary eye movements ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554411234
rs1554411234
Entrez Id: 1644;63979
Gene Symbol: DDC;FIGNL1
DDC;FIGNL1
CUI: C1847515
Disease:
Paroxysmal involuntary eye movements 		A 0.700 GeneticVariation CLINVAR