Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913482
rs121913482
FGFR3
CUI: C0022603
Disease: Seborrheic keratosis
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
dbSNP: rs121913482
rs121913482
FGFR3
CUI: C0022603
Disease: Seborrheic keratosis
Seborrheic keratosis 		T 0.800 CausalMutation CLINVAR