rs1799724, LTA;TNF

N. diseases: 45
Source: BEFREE ×
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.
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
603 0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 0.020 1.000 2 2015 2017
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
307 0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 0.020 0.500 2 2014 2014
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
616 0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 0.020 1.000 2 2015 2017
Achalasia
CUI: C1321756
Disease: Achalasia
5 0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 0.010 1.000 1 2014 2014
Adenocarcinoma
CUI: C0001418
Disease: Adenocarcinoma
167 0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 0.010 1.000 1 2017 2017
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
968 0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 0.010 1.000 1 2005 2005
Arthritis, Psoriatic
CUI: C0003872
Disease: Arthritis, Psoriatic
50 0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 0.010 1.000 1 2019 2019
Autoimmune Chronic Hepatitis
CUI: C0241910
Disease: Autoimmune Chronic Hepatitis
22 0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 0.010 1.000 1 2019 2019
Autoimmune hepatitis
CUI: C4721555
Disease: Autoimmune hepatitis
22 0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 0.010 1.000 1 2019 2019
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2145 0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 0.010 1.000 1 2013 2013
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
995 0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 0.010 1.000 1 2014 2014
Cardiac sarcoidosis
CUI: C0392077
Disease: Cardiac sarcoidosis
1 0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 0.010 1.000 1 2013 2013
Cerebral Palsy
CUI: C0007789
Disease: Cerebral Palsy
50 0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 0.010 1.000 1 2016 2016
cervical cancer
CUI: C4048328
Disease: cervical cancer
257 0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 0.010 1.000 1 2015 2015
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
266 0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 0.010 1.000 1 2015 2015
Chronic Kidney Diseases
CUI: C1561643
Disease: Chronic Kidney Diseases
155 0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 0.010 1.000 1 2009 2009
Complicated malaria
CUI: C2747816
Disease: Complicated malaria
38 0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 0.010 1.000 1 2007 2007
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
456 0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 0.010 1.000 1 2015 2015
Dementia
CUI: C0497327
Disease: Dementia
165 0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 0.010 1.000 1 2012 2012
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
1598 0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 0.010 1.000 1 2015 2015
Diabetic Retinopathy
CUI: C0011884
Disease: Diabetic Retinopathy
159 0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 0.010 1.000 1 2015 2015
Esophageal Achalasia
CUI: C0014848
Disease: Esophageal Achalasia
5 0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 0.010 1.000 1 2014 2014
Glaucoma
CUI: C0017601
Disease: Glaucoma
112 0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 0.010 1.000 1 2019 2019
Hepatitis B, Chronic
CUI: C0524909
Disease: Hepatitis B, Chronic
70 0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 0.010 1.000 1 2017 2017
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
316 0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 0.010 1.000 1 2016 2016