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.
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
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
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
Renal Cell Carcinoma
CUI: C0007134
Disease: Renal Cell Carcinoma
288 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1 2019 2019
Vitamin B 12 Deficiency
CUI: C0042847
Disease: Vitamin B 12 Deficiency
11 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1 2018 2018
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
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.060 0.833 6 2008 2019
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.080 0.875 8 2009 2018
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.080 0.875 8 2009 2018
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
261 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.030 1.000 3 2013 2017
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.030 1.000 3 2018 2019
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
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
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
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.020 1.000 2 2010 2012
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
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
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
Hyperhomocysteinemia
CUI: C0598608
Disease: Hyperhomocysteinemia
45 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.020 1.000 2 2018 2018
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