rs121913483, FGFR3

N. diseases: 31
Disease: Seborrheic keratosis ×
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
0.800 GeneticVariation UNIPROT Activating mutations of the tyrosine kinase receptor FGFR3 are associated with benign skin tumors in mice and humans. 15772091 2005
Seborrheic keratosis
CUI: C0022603
Disease: Seborrheic keratosis
0.800 CausalMutation CLINVAR