rs8179090, TIMP2

N. diseases: 12
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Androgen-Insensitivity Syndrome
CUI: C0039585
Disease: Androgen-Insensitivity Syndrome
176 0.752 0.280 17 78925807 upstream gene variant C/G snv 1.6E-02 0.010 1 2012 2012
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.752 0.280 17 78925807 upstream gene variant C/G snv 1.6E-02 0.010 1 2017 2017
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.752 0.280 17 78925807 upstream gene variant C/G snv 1.6E-02 0.010 1 2017 2017
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.752 0.280 17 78925807 upstream gene variant C/G snv 1.6E-02 0.010 1.000 1 2018 2018
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.752 0.280 17 78925807 upstream gene variant C/G snv 1.6E-02 0.010 1.000 1 2018 2018
Idiopathic scoliosis
CUI: C0595995
Disease: Idiopathic scoliosis
17 0.752 0.280 17 78925807 upstream gene variant C/G snv 1.6E-02 0.010 1 2019 2019
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.752 0.280 17 78925807 upstream gene variant C/G snv 1.6E-02 0.010 1.000 1 2016 2016
Malignant neoplasm of urinary bladder
316 0.752 0.280 17 78925807 upstream gene variant C/G snv 1.6E-02 0.010 1 2017 2017
MYELODYSPLASTIC SYNDROME
CUI: C3463824
Disease: MYELODYSPLASTIC SYNDROME
95 0.752 0.280 17 78925807 upstream gene variant C/G snv 1.6E-02 0.010 1.000 1 2016 2016
Ovarian Failure, Premature
CUI: C0085215
Disease: Ovarian Failure, Premature
115 0.752 0.280 17 78925807 upstream gene variant C/G snv 1.6E-02 0.010 1.000 1 2019 2019
Premature Menopause
CUI: C0025322
Disease: Premature Menopause
90 0.752 0.280 17 78925807 upstream gene variant C/G snv 1.6E-02 0.010 1.000 1 2019 2019
Tumor Cell Invasion
CUI: C1269955
Disease: Tumor Cell Invasion
169 0.752 0.280 17 78925807 upstream gene variant C/G snv 1.6E-02 0.010 1 2017 2017