rs121913274, PIK3CA

N. diseases: 33
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
0.700 GeneticVariation UNIPROT Oncogenic PIK3CA mutations occur in epidermal nevi and seborrheic keratoses with a characteristic mutation pattern. 17673550 2007