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 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
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
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
Bipolar Disorder
CUI: C0005586
Disease: Bipolar Disorder
839 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2008 2008
Blood Pressure
CUI: C0005823
Disease: Blood Pressure
220 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.700 1.000 1 2011 2011
Carcinoma, Basal Cell
CUI: C4721806
Disease: Carcinoma, Basal Cell
91 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2011 2011
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
Cerebral Palsy
CUI: C0007789
Disease: Cerebral Palsy
69 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2011 2011
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
Cognitive changes
CUI: C1392786
Disease: Cognitive changes
15 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2011 2011
Complete Trisomy 21 Syndrome
CUI: C4521042
Disease: Complete Trisomy 21 Syndrome
77 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2005 2005
Congenital omphalocele
CUI: C0795690
Disease: Congenital omphalocele
13 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2012 2012
Conventional (Clear Cell) Renal Cell Carcinoma
222 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1 2019 2019
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
Deep Vein Thrombosis
CUI: C0149871
Disease: Deep Vein Thrombosis
93 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2019 2019
Dementia, Vascular
CUI: C0011269
Disease: Dementia, Vascular
32 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2012 2012
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2012 2012
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2012 2012
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
Down Syndrome
CUI: C0013080
Disease: Down Syndrome
80 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2005 2005
Eclampsia
CUI: C0013537
Disease: Eclampsia
38 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2012 2012
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2011 2011
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2011 2011
Exfoliation Syndrome
CUI: C0206368
Disease: Exfoliation Syndrome
74 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1 2018 2018