Gene: IFT140 ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs779007169
rs779007169
IFT140
T 0.700 CausalMutation CLINVAR Impact of whole exome sequencing among Iranian patients with autosomal recessive retinitis pigmentosa. 26497376

2015
dbSNP: rs773372123
rs773372123
IFT140 ; LOC105371046
T 0.700 GeneticVariation CLINVAR