Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12329760
rs12329760
Entrez Id: 7113
Gene Symbol: TMPRSS2
TMPRSS2
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