rs1801133, MTHFR

N. diseases: 174
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.
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 0.100 1.000 16 2009 2020
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 0.100 1.000 16 2009 2020
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 0.100 0.818 11 2006 2019
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 0.090 1.000 9 1998 2018
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 0.070 0.857 7 2002 2016
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 0.070 1.000 7 2004 2018
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 0.760 1.000 7 2008 2017
Hyperhomocysteinemia
CUI: C0598608
Disease: Hyperhomocysteinemia
45 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 0.060 1.000 6 2013 2018
Neural Tube Defects
CUI: C0027794
Disease: Neural Tube Defects
122 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 0.060 1.000 6 2012 2019
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 0.050 1.000 5 2008 2016
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 0.050 0.800 5 2012 2019
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 0.050 1.000 5 2010 2018
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 0.040 1.000 4 2007 2019
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 0.040 1.000 4 2005 2018
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 0.040 1.000 4 2012 2018
Homocysteine measurement
CUI: C2242817
Disease: Homocysteine measurement
33 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 0.800 1.000 4 2009 2018
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 0.040 1.000 4 2009 2018
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 0.040 0.500 4 2018 2019
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 0.040 1.000 4 2007 2019
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 0.040 1.000 4 2007 2019
Aortic Aneurysm, Abdominal
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
90 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 0.030 1.000 3 2014 2015
Childhood Acute Lymphoblastic Leukemia
261 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 0.030 1.000 3 2015 2017
Conventional (Clear Cell) Renal Cell Carcinoma
222 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 0.030 0.667 3 2008 2019
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 0.030 1.000 3 2012 2018
Malignant neoplasm of colon and/or rectum
502 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 0.030 1.000 3 2011 2017