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.
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
Experimental Organism Basal Cell Carcinoma
63 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2011 2011
Fanconi Anemia
CUI: C0015625
Disease: Fanconi Anemia
173 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1 2018 2018
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
194 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1 2018 2018
FRIEDREICH ATAXIA 1
CUI: C1856689
Disease: FRIEDREICH ATAXIA 1
24 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1 2018 2018
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
Glaucoma
CUI: C0017601
Disease: Glaucoma
198 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2019 2019
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
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
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
Intellectual Disability
CUI: C3714756
Disease: Intellectual Disability
159 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2011 2011
Kidney Diseases
CUI: C0022658
Disease: Kidney Diseases
140 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2012 2012
Lip and Oral Cavity Carcinoma
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
172 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2011 2011
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
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
Male infertility
CUI: C0021364
Disease: Male infertility
146 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2012 2012
Malignant neoplasm of colon and/or rectum
502 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2011 2011
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2011 2011
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
Malignant neoplasm of mouth
CUI: C0153381
Disease: Malignant neoplasm of mouth
184 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2011 2011
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2010 2010
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
Mental Retardation
CUI: C0025362
Disease: Mental Retardation
98 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2011 2011