rs12329760, TMPRSS2

N. diseases: 3
Disease: Familial lichen amyloidosis ×
Source: BEFREE ×
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Familial lichen amyloidosis
CUI: C0268398
Disease: Familial lichen amyloidosis
0.010 GeneticVariation BEFREE The T-allele of the Met160Val variant in TMPRSS2, which has been associated with the TMPRSS2-ERG fusion, may be informative of time to PCA diagnosis for a subset of high-risk Caucasian men who are undergoing regular PCA screening. 20735386 2011