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.
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: 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
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
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 0.010 1.000 1 2008 2008
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 0.020 1.000 2 2012 2016
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 0.020 1.000 2 2012 2016
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
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
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
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
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 0.010 1.000 1 2014 2014
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 0.010 1 2014 2014
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
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
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
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
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
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
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
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
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 0.010 1.000 1 2016 2016
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 0.010 1.000 1 2016 2016
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 0.010 1.000 1 2016 2016
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