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.
Adult Meningioma
CUI: C0278877
Disease: Adult Meningioma
30 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.020 1.000 2 2017 2017
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.020 1.000 2 2012 2017
Meningioma
CUI: C0025286
Disease: Meningioma
43 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.020 1.000 2 2017 2017
Meningioma, benign, no ICD-O subtype
30 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.020 1.000 2 2017 2017
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.020 0.500 2 2010 2017
Anterior encephalocele
CUI: C4024948
Disease: Anterior encephalocele
5 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2017 2017
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2017 2017
Gestational Trophoblastic Neoplasms
CUI: C1135868
Disease: Gestational Trophoblastic Neoplasms
7 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2017 2017
Glioma
CUI: C0017638
Disease: Glioma
353 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2017 2017
Hyperactive behavior
CUI: C0424295
Disease: Hyperactive behavior
112 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2017 2017
Impulsive Behavior
CUI: C0021125
Disease: Impulsive Behavior
69 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2017 2017
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2017 2017
Factor V Leiden mutation
CUI: C0584960
Disease: Factor V Leiden mutation
46 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.020 1.000 2 2012 2016
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
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
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.030 1.000 3 2010 2014
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
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