rs1805087, MTR

N. diseases: 135
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.
Neural Tube Defects
CUI: C0027794
Disease: Neural Tube Defects
122 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.090 0.667 9 1997 2018
Vascular Diseases
CUI: C0042373
Disease: Vascular Diseases
40 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.020 0.500 2 1997 1999
Adenoma of large intestine
CUI: C1302401
Disease: Adenoma of large intestine
213 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.050 0.800 5 1998 2013
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.080 1.000 8 1999 2017
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.050 0.600 5 1999 2013
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.020 1.000 2 1999 2004
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2000 2000
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.080 1.000 8 2001 2019
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.050 0.800 5 2001 2012
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.030 1.000 3 2001 2005
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.020 1.000 2 2001 2007
Chronic kidney disease stage 5
CUI: C2316810
Disease: Chronic kidney disease stage 5
194 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2001 2001
Kidney Failure, Chronic
CUI: C0022661
Disease: Kidney Failure, Chronic
425 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2001 2001
Adult Acute Lymphocytic Leukemia
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
154 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.040 1.000 4 2002 2012
Hyperhomocysteinemia
CUI: C0598608
Disease: Hyperhomocysteinemia
45 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.030 1.000 3 2002 2017
Atherothrombosis
CUI: C1963943
Disease: Atherothrombosis
15 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2002 2002
Down Syndrome
CUI: C0013080
Disease: Down Syndrome
80 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.100 0.833 12 2003 2014
Complete Trisomy 21 Syndrome
CUI: C4521042
Disease: Complete Trisomy 21 Syndrome
77 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.100 0.818 11 2003 2014
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.040 0.750 4 2003 2008
Lymphoma, Non-Hodgkin
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
197 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.040 1.000 4 2003 2015
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.030 0.667 3 2003 2008
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.020 1.000 2 2003 2010
B-Cell Lymphomas
CUI: C0079731
Disease: B-Cell Lymphomas
42 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2003 2003
Adult Lymphoma
CUI: C1332206
Disease: Adult Lymphoma
66 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.030 0.333 3 2004 2017
Childhood Lymphoma
CUI: C1332979
Disease: Childhood Lymphoma
66 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.030 0.333 3 2004 2017