rs1801131, MTHFR

N. diseases: 93
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.
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.020 1.000 2 2016 2019
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2016 2016
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2016 2016
Retinoblastoma
CUI: C0035335
Disease: Retinoblastoma
193 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2016 2016
Retinopathy of Prematurity
CUI: C0035344
Disease: Retinopathy of Prematurity
16 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2016 2016
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.020 1.000 2 2015 2018
Acrocyanosis
CUI: C0221347
Disease: Acrocyanosis
5 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2015 2015
AIDS related complex
CUI: C0001857
Disease: AIDS related complex
43 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2015 2015
Attention deficit hyperactivity disorder
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
420 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.020 1.000 2 2014 2018
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.020 1.000 2 2014 2014
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.020 1.000 2 2014 2019
adult chronic myelogenous leukemia
CUI: C4733577
Disease: adult chronic myelogenous leukemia
3 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2014 2014
Adult Liver Carcinoma
CUI: C0220630
Disease: Adult Liver Carcinoma
72 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2014 2014
Cognition Disorders
CUI: C0009241
Disease: Cognition Disorders
47 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2014 2014
Diffuse Large B-Cell Lymphoma
CUI: C0079744
Disease: Diffuse Large B-Cell Lymphoma
127 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2014 2014
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
348 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2014 2014
Liver and Intrahepatic Biliary Tract Carcinoma
CUI: C0279000
Disease: Liver and Intrahepatic Biliary Tract Carcinoma
73 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2014 2014
Malignant neoplasm of liver
CUI: C0345904
Disease: Malignant neoplasm of liver
88 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2014 2014
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2014 2014
Myeloid Leukemia
CUI: C0023470
Disease: Myeloid Leukemia
7 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2014 2014
Thrombocytopenia
CUI: C0040034
Disease: Thrombocytopenia
110 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2014 2014
Acute lymphocytic leukemia
CUI: C0023449
Disease: Acute lymphocytic leukemia
222 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.030 1.000 3 2013 2017
Adult Acute Lymphocytic Leukemia
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
154 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.030 1.000 3 2013 2017
Childhood Acute Lymphoblastic Leukemia
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
261 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.030 1.000 3 2013 2017
Meniere Disease
CUI: C0025281
Disease: Meniere Disease
36 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2013 2013