rs1001179, CAT

N. diseases: 33
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.
Acoustic Neuroma
CUI: C0027859
Disease: Acoustic Neuroma
3 0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 0.010 1.000 1 2008 2008
Prostatic Diseases
CUI: C0033575
Disease: Prostatic Diseases
4 0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 0.010 1.000 1 2012 2012
Stage IV Prostate Cancer AJCC v7
CUI: C3146264
Disease: Stage IV Prostate Cancer AJCC v7
6 0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 0.010 1.000 1 2015 2015
Stage IV Prostate Cancer AJCC v8
CUI: C4553752
Disease: Stage IV Prostate Cancer AJCC v8
6 0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 0.010 1.000 1 2015 2015
Stage IV Prostate Carcinoma
CUI: C0278837
Disease: Stage IV Prostate Carcinoma
6 0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 0.010 1.000 1 2015 2015
Hypoxic-Ischemic Encephalopathy
CUI: C0752304
Disease: Hypoxic-Ischemic Encephalopathy
12 0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 0.010 1.000 1 2016 2016
Malignant mesothelioma
CUI: C0345967
Disease: Malignant mesothelioma
12 0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 0.010 1 2018 2018
Diabetic peripheral neuropathy
CUI: C0740447
Disease: Diabetic peripheral neuropathy
16 0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 0.010 1.000 1 2018 2018
Alcohol abuse
CUI: C0085762
Disease: Alcohol abuse
24 0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 0.010 1.000 1 2017 2017
Neurologic Symptoms
CUI: C0235031
Disease: Neurologic Symptoms
30 0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 0.010 1.000 1 2015 2015
Dyskinetic syndrome
CUI: C0013384
Disease: Dyskinetic syndrome
42 0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 0.010 1.000 1 2019 2019
Primary angle-closure glaucoma
CUI: C0017606
Disease: Primary angle-closure glaucoma
55 0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 0.010 1.000 1 2013 2013
Angle Closure Glaucoma
CUI: C0017605
Disease: Angle Closure Glaucoma
56 0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 0.010 1.000 1 2013 2013
Fibrosis, Liver
CUI: C0239946
Disease: Fibrosis, Liver
64 0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 0.010 1.000 1 2016 2016
Cerebral Palsy
CUI: C0007789
Disease: Cerebral Palsy
69 0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 0.010 1.000 1 2016 2016
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
92 0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 0.010 1.000 1 2017 2017
Glaucoma, Primary Open Angle
CUI: C0339573
Disease: Glaucoma, Primary Open Angle
222 0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 0.020 0.500 2 2013 2018
Vitiligo
CUI: C0042900
Disease: Vitiligo
249 0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 0.010 1.000 1 2017 2017
Hepatolenticular Degeneration
CUI: C0019202
Disease: Hepatolenticular Degeneration
349 0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 0.010 1.000 1 2015 2015
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
363 0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 0.010 1 2018 2018
Chronic Obstructive Airway Disease
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
852 0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 0.010 1.000 1 2019 2019
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 0.010 1.000 1 2016 2016
Diabetes Mellitus, Insulin-Dependent
954 0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 0.020 0.500 2 2006 2018
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 0.010 1.000 1 2019 2019
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 0.010 1.000 1 2016 2016