TMPRSS2, transmembrane serine protease 2, 7113

N. diseases: 69; N. variants: 3
Source: ALL
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: C0376358
Disease:
Malignant neoplasm of prostate 		0.030 GeneticVariation BEFREE The TMPRSS2 Met160Val polymorphism is a genetic risk factor for sporadic prostate cancer in a Japanese population. 25040002 2014
dbSNP: rs12329760
rs12329760
Entrez Id: 7113
Gene Symbol: TMPRSS2
TMPRSS2
CUI: C0600139
Disease:
Prostate carcinoma 		0.030 GeneticVariation BEFREE The TMPRSS2 Met160Val polymorphism is a genetic risk factor for sporadic prostate cancer in a Japanese population. 25040002 2014
dbSNP: rs12329760
rs12329760
Entrez Id: 7113
Gene Symbol: TMPRSS2
TMPRSS2
CUI: C0600139
Disease:
Prostate carcinoma 		0.030 GeneticVariation BEFREE Racial differences in prediction of time to prostate cancer diagnosis in a prospective screening cohort of high-risk men: effect of TMPRSS2 Met160Val. 20735386 2011
dbSNP: rs12329760
rs12329760
Entrez Id: 7113
Gene Symbol: TMPRSS2
TMPRSS2
CUI: C0376358
Disease:
Malignant neoplasm of prostate 		0.030 GeneticVariation BEFREE Racial differences in prediction of time to prostate cancer diagnosis in a prospective screening cohort of high-risk men: effect of TMPRSS2 Met160Val. 20735386 2011
dbSNP: rs12329760
rs12329760
Entrez Id: 7113
Gene Symbol: TMPRSS2
TMPRSS2
CUI: C0600139
Disease:
Prostate carcinoma 		0.030 GeneticVariation BEFREE Met160Val polymorphism in the TRMPSS2 gene and risk of prostate cancer in a population-based case-control study. 15065083 2004
dbSNP: rs12329760
rs12329760
Entrez Id: 7113
Gene Symbol: TMPRSS2
TMPRSS2
CUI: C0376358
Disease:
Malignant neoplasm of prostate 		0.030 GeneticVariation BEFREE Met160Val polymorphism in the TRMPSS2 gene and risk of prostate cancer in a population-based case-control study. 15065083 2004
dbSNP: rs2070788
rs2070788
Entrez Id: 7113
Gene Symbol: TMPRSS2
TMPRSS2
CUI: C3665951
Disease:
Influenza due to Influenza A virus subtype H7N9 		0.010 GeneticVariation BEFREE Notably, rs2070788 and rs383510 were significantly associated with the susceptibility to A(H7N9) influenza in 102 patients with A(H7N9) influenza and 106 healthy controls. 25904605 2015
dbSNP: rs383510
rs383510
Entrez Id: 7113
Gene Symbol: TMPRSS2
TMPRSS2
CUI: C3665951
Disease:
Influenza due to Influenza A virus subtype H7N9 		0.010 GeneticVariation BEFREE Notably, rs2070788 and rs383510 were significantly associated with the susceptibility to A(H7N9) influenza in 102 patients with A(H7N9) influenza and 106 healthy controls. 25904605 2015
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