IFT57, intraflagellar transport 57, 55081

N. diseases: 31; N. variants: 1
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1560127636
rs1560127636
Entrez Id: 55081
Gene Symbol: IFT57
IFT57
CUI: C4693651
Disease:
OROFACIODIGITAL SYNDROME XVIII 		C 0.700 GeneticVariation CLINVAR