IFT80, intraflagellar transport 80, 57560

N. diseases: 109; N. variants: 10
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs138004478
rs138004478
Entrez Id: 57560;100174949
Gene Symbol: IFT80;TRIM59-IFT80
IFT80;TRIM59-IFT80
CUI: C0265275
Disease:
Jeune thoracic dystrophy
G 0.700 CausalMutation CLINVAR
dbSNP: rs1553753582
rs1553753582
Entrez Id: 57560;100174949
Gene Symbol: IFT80;TRIM59-IFT80
IFT80;TRIM59-IFT80
CUI: C0265275
Disease:
Jeune thoracic dystrophy
A 0.700 CausalMutation CLINVAR
dbSNP: rs372576954
rs372576954
Entrez Id: 57560;100174949
Gene Symbol: IFT80;TRIM59-IFT80
IFT80;TRIM59-IFT80
CUI: C0265275
Disease:
Jeune thoracic dystrophy
T 0.700 CausalMutation CLINVAR