rs78311289, FGFR3

N. diseases: 25
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Seborrheic keratosis
CUI: C0022603
Disease: Seborrheic keratosis
0.700 GeneticVariation UNIPROT Activating mutations of the tyrosine kinase receptor FGFR3 are associated with benign skin tumors in mice and humans. 15772091 2005